Jobs at MMR CONSULTING (Now Hiring) — 16 open

Biopharmaceutical - CQV Lead/ PROJECT MANAGER

Raleigh, North Carolina, United States · On-site

Senior+

Previous Pharmaceutical/Biotech experience is mandatory for this role. MMR Consulting is a consulting firm specializing in the pharmaceutical and biotechnology industries. Our services include Project Management, Process…

Skills: Project Management, Commissioning And Qualification, cGMP, Capital Projects, Greenfield Projects

MMR CONSULTING

Biopharmaceutical - CQV PROJECT DIRECTOR

Guaynabo, Puerto Rico, United States · On-site

$110k–$150k/yr

Senior+

Skills: Project Management, Commissioning And Qualification, Capital Projects Management, cGMP Operations, Greenfield Projects

MMR CONSULTING

PHARMACEUTICAL – SR. CQV Manager/PM

Guaynabo, Puerto Rico, United States · On-site

$120k–$150k/yr

Senior+

Previous Pharmaceutical/Biotech experience is mandatory for this role (Commissioning, Qualification & Validation – Pharmaceutical Manufacturing) The work will require 90% travel to work in Denver/Boulder, Raleigh, midwes…

Skills: Commissioning, Qualification & Validation, Project Management, GMP Compliance, FDA Regulations, Risk Assessment

MMR CONSULTING

PHARMACEUTICAL – SR. CQV ENGINEER

Irvine, California, United States · On-site

$100k–$115k/yr

Senior+

Previous Pharmaceutical/Biotech experience is mandatory for this role MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering…

Skills: Commissioning, Qualification, Validation, cGMP, Project Management

MMR CONSULTING

Biopharmaceutical - CQV Lead/ PROJECT MANAGER

Raleigh, North Carolina, United States · On-site

Senior+

Skills: Project Management, Commissioning And Qualification, CQV, cGMP, Capital Projects

MMR CONSULTING

Engineering Pharma Technical Recruiter (remote)

Tijuana, Baja California, Mexico · Remote OK

Senior+

This role is 100% remote. Recruiting primarily for US & Canada roles. Excellent English communication skills are required. MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical /biotechn…

Skills: Full-cycle Recruitment, Technical Sourcing, Candidate Screening, Talent Pipeline Building, Interview Coordination

MMR CONSULTING

Engineering Pharma Technical Recruiter (remote)

Cuernavaca, Morelos, Mexico · Remote OK

Senior+

Skills: Full-cycle Recruitment, Technical Sourcing, Candidate Screening, Interview Coordination, Talent Pipeline Building

MMR CONSULTING

Engineering Pharma Technical Recruiter (remote)

Mexico City, Mexico · Remote OK

Senior+

Skills: Full-cycle Recruitment, Technical Sourcing, Candidate Screening, Talent Pipeline Building, Interview Coordination

MMR CONSULTING

Engineering Pharma Technical Recruiter (remote)

Guadalajara, Jalisco, Mexico · Remote OK

Senior+

Skills: Full-cycle Recruitment, Technical Sourcing, Candidate Screening, Talent Pipeline Building, Interview Coordination

MMR CONSULTING

Biotechnology - Building Automation Systems Engineer (Siemens)

Tijuana, Baja California, Mexico · On-site

SeniorVisa sponsorship

Previous Pharmaceutical/Biotech experience is mandatory for this role. MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineerin…

Skills: Siemens Insight, Siemens Desigo, Building Automation Systems, Electrical Drawing Review, BAS Programming

MMR CONSULTING

Biotechnology - Building Automation Systems Engineer (Siemens)

Mexico City, Mexico · On-site

SeniorVisa sponsorship

Skills: Building Automation Systems, Siemens Insight, Siemens Desigo, Electrical Drawing Review, BAS Programming

MMR CONSULTING

Biotechnology - Building Automation Systems Engineer (Siemens)

Guadalajara, Jalisco, Mexico · On-site

SeniorVisa sponsorship

Skills: Siemens Insight, Siemens Desigo, Building Automation Systems, Electrical Drawing Review, BAS Programming

MMR CONSULTING

Biotechnology - Building Automation Systems Engineer (Siemens)

Cuernavaca, Morelos, Mexico · On-site

SeniorVisa sponsorship

Skills: Building Automation Systems, Siemens Insight, Siemens Desigo, Project Management, Commissioning

MMR CONSULTING

PHARMACEUTICAL – SR. CQV ENGINEER

Carlsbad, California, United States · On-site

$100k–$115k/yr

Senior+

Skills: Commissioning, Qualification, Validation, cGMP, Project Management

MMR CONSULTING

BIOPHARMACEUTICAL – C&Q Manager

Boulder, Colorado, United States · On-site

$90k–$145k/yr

Senior+

Skills: Commissioning & Qualification, Validation, Bioprocess Systems, Project Management, Leadership

MMR CONSULTING

Biopharmaceutical CQV SPECIALIST

Raleigh, North Carolina, United States · On-site

$80k–$100k/yr

Mid level

Skills: Commissioning, Qualification, Validation, cGMP, Project Management

Biopharmaceutical - CQV Lead/ PROJECT MANAGER

MMR CONSULTING

Raleigh, North Carolina, United States • On-site

Apply

Senior+

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Full-time
bachelor degree
Posted 21d ago
~40 hrs/week

Responsibilities

Lead the design, commissioning, qualification, and project management of biopharmaceutical equipment and facilities from feasibility to handover. Coordinate cross-functional departments and manage external vendors to ensure successful project execution and safety compliance.

Requirements

Requires over 10 years of biotech industry experience in project management, specifically with cGMP, capital, and greenfield projects. A degree in Mechanical, Chemical, or Electrical engineering is preferred, along with leadership and mentorship skills.

Full job description

Previous Pharmaceutical/Biotech experience is mandatory for this role.

MMR Consulting is a consulting firm specializing in the pharmaceutical and biotechnology industries. Our services include Project Management, Process, Automation, Facilities and Equipment CQV.

MMR Consulting has offices in Canada, USA, and Australia.

This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of specialists involved in project management, commissioning and qualification, of equipment, systems and facilities.

This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of specialists involved in the design, commissioning & qualification, start-up and project management of various processes, systems and facilities. The work will require working out of client’s facilities.

The work will require working out of the client’s facilities in Raleigh, North Carolina.

Responsibilities

Provide technical guidance into the assessments, design, project management, commissioning and start-up of equipment and facilities, for upgrades, renovations and expansions of client facilities and processes.
Lead or support project execution from feasibility through to project completion/handover, including all project stages such as:

Feasibility Assessments

Concept Design, Basic Design, Detailed Design

Procurement

Construction / Installation

Project Controls - Monitoring

Commissioning & Qualification

Prepare business cases, with project purpose, risks, budget, schedule, resource requirements.
Manage other design firms, equipment vendors, construction firms and internal / external stakeholders as required to execute projects.
Manage Capital Projects
Review technical documentation such as P&IDs, specifications, layouts, manuals, datasheets.
Integrate safety into the design and execution of all projects (HAZOP reviews, PHSRs, design reviews with EHS representatives).
Prepare/review automation sequences, as required for Process Automation.
Engage and coordinate with other other cross-functional departments (Process, automation, building / facilities, procurement, construction management, commissioning, qualification & validation, manufacturing operations, EHS, quality & compliance).
Facilitate project management tools throughout the execution of projects, such as procurement tracking, vendor management, meeting minutes / action lists, risk register log, schedule updates, project updates.
Coordinate meetings with cross-functional departments, to drive project progress, facilitate decisions, provide updates.
Travel may be occasionally required for meetings with equipment fabrication vendors or Factory Acceptance Testing (FATs).
Work may require occasional support over shutdowns or extended hours, specifically during installation, construction, commissioning, qualification & validation phases.
You may be involved with other aspects such as client-management (maintain key Client relationships in support of business development and pursuit of new work), project scheduling/budgeting, coordination of client and MMR resources for effective project delivery, supporting business development (providing technical support to the sales as required for proposals/opportunities), presenting at industry conferences/publishing papers etc.
Visit construction and installation sites, wear necessary safety PPE.
Supervise contractors during critical installations of process equipment and associated utilities.
Other duties as assigned by client, and/or MMR, based on workload and project requirements.
As this position requires working on client sites, you will need to comply with the client’s safety rules including mandatory vaccination policies for COVID-19, where applicable.

Qualifications

10+ years of experience in the biotech industry in project management of various equipment and facilities within the pharmaceutical/biotech industry, with knowledge of requirements for a cGMP operation.
Previous PM capital projects experience is required.
Previous Greenfield projects experience is required.
Possess leadership skills, and be able to take initiative to lead projects, involving multiple stakeholders, departments, and varying complexity.
Possess mentorship skills, to coach and develop junior and intermediate employees.
Basic knowledge of AutoCAD.
Degree, preferably in Mechanical, Chemical, Electrical or other industry related discipline.
Certification in Project Management would be an asset.
Travel may be required on occasion. Ability to travel to the US would be an asset.

Equal Employment Opportunity and Reasonable Accommodations

MMR Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our hiring decisions are based on merit, qualifications, and business needs. We are committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please let us know the nature of your request.

Related keywords

BiopharmaceuticalCQVProject ManagementcGMPGreenfield ProjectsCapital ProjectsP&IDHAZOPPHSREHSFATAutoCADCommissioningQualificationValidationProcess Automation

About MMR CONSULTING

LinkedIn Visit site

Pharma Consulting: Engineering, Project Management, Compliance, Validation

Industry: Biotechnology Research
Company size: 51-200 employees
Founded: 2017
Headquarters: Carlsbad, California
LinkedIn followers: 16,902

MMR Consulting Inc. and its dedicated team of experienced consultants are committed to delivering high quality, robust solutions for the Pharmaceutical and Biotechnology industries. Our expertise includes Engineering (Process, Automation, Facilities), Capital Project Management of large/complex projects and programs, Commissioning Qualification Validation, and GMP Compliance services.

Offices: Loker Ave E, Suite 110, Carlsbad, California 92010, US · 2500 Regency Pkwy, Raleigh, North Carolina, US · 15255 S 94th Ave, 5, Chicago, Illinois 60462, US · 81 Zenway Blvd, 3, Toronto, Ontario L4H 0S5, CA · 171 Clarence St, 10, Australia, New South Wales 2000, AU

Capital Project ManagementCapital Project Controlsand Construction ManagementBiotechnologyManagement ConsultingLife ScienceIndustrial Automation

View all jobs at MMR CONSULTING

About MMR CONSULTING

LinkedIn Visit site

Pharma Consulting: Engineering, Project Management, Compliance, Validation

Industry: Biotechnology Research
Company size: 51-200 employees
Founded: 2017
Headquarters: Carlsbad, California
LinkedIn followers: 16,902

Capital Project ManagementCapital Project Controlsand Construction ManagementBiotechnologyManagement ConsultingLife ScienceIndustrial Automation

View all jobs at MMR CONSULTING

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Jobs at MMR CONSULTING (Now Hiring) — 16 open

MMR CONSULTING

Biopharmaceutical - CQV Lead/ PROJECT MANAGER

Raleigh, North Carolina, United States · On-site

Senior+

Skills: Project Management, Commissioning And Qualification, cGMP, Capital Projects, Greenfield Projects

MMR CONSULTING

Biopharmaceutical - CQV PROJECT DIRECTOR

Guaynabo, Puerto Rico, United States · On-site

$110k–$150k/yr

Senior+

Skills: Project Management, Commissioning And Qualification, Capital Projects Management, cGMP Operations, Greenfield Projects

MMR CONSULTING

PHARMACEUTICAL – SR. CQV Manager/PM

Guaynabo, Puerto Rico, United States · On-site

$120k–$150k/yr

Senior+

Skills: Commissioning, Qualification & Validation, Project Management, GMP Compliance, FDA Regulations, Risk Assessment

MMR CONSULTING

PHARMACEUTICAL – SR. CQV ENGINEER

Irvine, California, United States · On-site

$100k–$115k/yr

Senior+

Skills: Commissioning, Qualification, Validation, cGMP, Project Management

MMR CONSULTING

Biopharmaceutical - CQV Lead/ PROJECT MANAGER

Raleigh, North Carolina, United States · On-site

Senior+

Skills: Project Management, Commissioning And Qualification, CQV, cGMP, Capital Projects

MMR CONSULTING

Engineering Pharma Technical Recruiter (remote)

Tijuana, Baja California, Mexico · Remote OK

Senior+

Skills: Full-cycle Recruitment, Technical Sourcing, Candidate Screening, Talent Pipeline Building, Interview Coordination

MMR CONSULTING

Engineering Pharma Technical Recruiter (remote)

Cuernavaca, Morelos, Mexico · Remote OK

Senior+

Skills: Full-cycle Recruitment, Technical Sourcing, Candidate Screening, Interview Coordination, Talent Pipeline Building

MMR CONSULTING

Engineering Pharma Technical Recruiter (remote)

Mexico City, Mexico · Remote OK

Senior+

Skills: Full-cycle Recruitment, Technical Sourcing, Candidate Screening, Talent Pipeline Building, Interview Coordination

MMR CONSULTING

Engineering Pharma Technical Recruiter (remote)

Guadalajara, Jalisco, Mexico · Remote OK

Senior+

Skills: Full-cycle Recruitment, Technical Sourcing, Candidate Screening, Talent Pipeline Building, Interview Coordination

MMR CONSULTING

Biotechnology - Building Automation Systems Engineer (Siemens)

Tijuana, Baja California, Mexico · On-site

SeniorVisa sponsorship

Skills: Siemens Insight, Siemens Desigo, Building Automation Systems, Electrical Drawing Review, BAS Programming

MMR CONSULTING

Biotechnology - Building Automation Systems Engineer (Siemens)

Mexico City, Mexico · On-site

SeniorVisa sponsorship

Skills: Building Automation Systems, Siemens Insight, Siemens Desigo, Electrical Drawing Review, BAS Programming

MMR CONSULTING

Biotechnology - Building Automation Systems Engineer (Siemens)

Guadalajara, Jalisco, Mexico · On-site

SeniorVisa sponsorship

Skills: Siemens Insight, Siemens Desigo, Building Automation Systems, Electrical Drawing Review, BAS Programming

MMR CONSULTING

Biotechnology - Building Automation Systems Engineer (Siemens)

Cuernavaca, Morelos, Mexico · On-site

SeniorVisa sponsorship

Skills: Building Automation Systems, Siemens Insight, Siemens Desigo, Project Management, Commissioning

MMR CONSULTING

PHARMACEUTICAL – SR. CQV ENGINEER

Carlsbad, California, United States · On-site

$100k–$115k/yr

Senior+

Skills: Commissioning, Qualification, Validation, cGMP, Project Management

MMR CONSULTING

BIOPHARMACEUTICAL – C&Q Manager

Boulder, Colorado, United States · On-site

$90k–$145k/yr

Senior+

Skills: Commissioning & Qualification, Validation, Bioprocess Systems, Project Management, Leadership

MMR CONSULTING

Biopharmaceutical CQV SPECIALIST

Raleigh, North Carolina, United States · On-site

$80k–$100k/yr

Mid level

Skills: Commissioning, Qualification, Validation, cGMP, Project Management

Biopharmaceutical - CQV Lead/ PROJECT MANAGER

MMR CONSULTING

Raleigh, North Carolina, United States • On-site

Apply

Senior+

Tired of cold applications?

Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.

Full-time
bachelor degree
Posted 21d ago
~40 hrs/week

Responsibilities

Requirements

Full job description

Previous Pharmaceutical/Biotech experience is mandatory for this role.

MMR Consulting is a consulting firm specializing in the pharmaceutical and biotechnology industries. Our services include Project Management, Process, Automation, Facilities and Equipment CQV.

MMR Consulting has offices in Canada, USA, and Australia.

The work will require working out of the client’s facilities in Raleigh, North Carolina.

Responsibilities

Provide technical guidance into the assessments, design, project management, commissioning and start-up of equipment and facilities, for upgrades, renovations and expansions of client facilities and processes.
Lead or support project execution from feasibility through to project completion/handover, including all project stages such as:

Feasibility Assessments

Concept Design, Basic Design, Detailed Design

Procurement

Construction / Installation

Project Controls - Monitoring

Commissioning & Qualification

Prepare business cases, with project purpose, risks, budget, schedule, resource requirements.
Manage other design firms, equipment vendors, construction firms and internal / external stakeholders as required to execute projects.
Manage Capital Projects
Review technical documentation such as P&IDs, specifications, layouts, manuals, datasheets.
Integrate safety into the design and execution of all projects (HAZOP reviews, PHSRs, design reviews with EHS representatives).
Prepare/review automation sequences, as required for Process Automation.
Engage and coordinate with other other cross-functional departments (Process, automation, building / facilities, procurement, construction management, commissioning, qualification & validation, manufacturing operations, EHS, quality & compliance).
Facilitate project management tools throughout the execution of projects, such as procurement tracking, vendor management, meeting minutes / action lists, risk register log, schedule updates, project updates.
Coordinate meetings with cross-functional departments, to drive project progress, facilitate decisions, provide updates.
Travel may be occasionally required for meetings with equipment fabrication vendors or Factory Acceptance Testing (FATs).
Work may require occasional support over shutdowns or extended hours, specifically during installation, construction, commissioning, qualification & validation phases.
You may be involved with other aspects such as client-management (maintain key Client relationships in support of business development and pursuit of new work), project scheduling/budgeting, coordination of client and MMR resources for effective project delivery, supporting business development (providing technical support to the sales as required for proposals/opportunities), presenting at industry conferences/publishing papers etc.
Visit construction and installation sites, wear necessary safety PPE.
Supervise contractors during critical installations of process equipment and associated utilities.
Other duties as assigned by client, and/or MMR, based on workload and project requirements.
As this position requires working on client sites, you will need to comply with the client’s safety rules including mandatory vaccination policies for COVID-19, where applicable.

Qualifications

10+ years of experience in the biotech industry in project management of various equipment and facilities within the pharmaceutical/biotech industry, with knowledge of requirements for a cGMP operation.
Previous PM capital projects experience is required.
Previous Greenfield projects experience is required.
Possess leadership skills, and be able to take initiative to lead projects, involving multiple stakeholders, departments, and varying complexity.
Possess mentorship skills, to coach and develop junior and intermediate employees.
Basic knowledge of AutoCAD.
Degree, preferably in Mechanical, Chemical, Electrical or other industry related discipline.
Certification in Project Management would be an asset.
Travel may be required on occasion. Ability to travel to the US would be an asset.

Equal Employment Opportunity and Reasonable Accommodations

Related keywords

BiopharmaceuticalCQVProject ManagementcGMPGreenfield ProjectsCapital ProjectsP&IDHAZOPPHSREHSFATAutoCADCommissioningQualificationValidationProcess Automation

About MMR CONSULTING

LinkedIn Visit site

Pharma Consulting: Engineering, Project Management, Compliance, Validation

Industry: Biotechnology Research
Company size: 51-200 employees
Founded: 2017
Headquarters: Carlsbad, California
LinkedIn followers: 16,902

Capital Project ManagementCapital Project Controlsand Construction ManagementBiotechnologyManagement ConsultingLife ScienceIndustrial Automation

View all jobs at MMR CONSULTING

About MMR CONSULTING

LinkedIn Visit site

Pharma Consulting: Engineering, Project Management, Compliance, Validation

Industry: Biotechnology Research
Company size: 51-200 employees
Founded: 2017
Headquarters: Carlsbad, California
LinkedIn followers: 16,902

Capital Project ManagementCapital Project Controlsand Construction ManagementBiotechnologyManagement ConsultingLife ScienceIndustrial Automation

View all jobs at MMR CONSULTING

Jobs at MMR CONSULTING (Now Hiring) — 16 open

Biopharmaceutical - CQV Lead/ PROJECT MANAGER

Biopharmaceutical - CQV PROJECT DIRECTOR

PHARMACEUTICAL – SR. CQV Manager/PM

PHARMACEUTICAL – SR. CQV ENGINEER

Biopharmaceutical - CQV Lead/ PROJECT MANAGER

Engineering Pharma Technical Recruiter (remote)

Engineering Pharma Technical Recruiter (remote)

Engineering Pharma Technical Recruiter (remote)

Engineering Pharma Technical Recruiter (remote)

Biotechnology - Building Automation Systems Engineer (Siemens)

Biotechnology - Building Automation Systems Engineer (Siemens)

Biotechnology - Building Automation Systems Engineer (Siemens)

Biotechnology - Building Automation Systems Engineer (Siemens)

PHARMACEUTICAL – SR. CQV ENGINEER

BIOPHARMACEUTICAL – C&Q Manager

Biopharmaceutical CQV SPECIALIST

Biopharmaceutical - CQV Lead/ PROJECT MANAGER

Tired of cold applications?

Responsibilities

Requirements

Full job description

Related keywords

About MMR CONSULTING

About MMR CONSULTING

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Jobs at MMR CONSULTING (Now Hiring) — 16 open

Biopharmaceutical - CQV Lead/ PROJECT MANAGER

Biopharmaceutical - CQV PROJECT DIRECTOR

PHARMACEUTICAL – SR. CQV Manager/PM

PHARMACEUTICAL – SR. CQV ENGINEER

Biopharmaceutical - CQV Lead/ PROJECT MANAGER

Engineering Pharma Technical Recruiter (remote)

Engineering Pharma Technical Recruiter (remote)

Engineering Pharma Technical Recruiter (remote)

Engineering Pharma Technical Recruiter (remote)

Biotechnology - Building Automation Systems Engineer (Siemens)

Biotechnology - Building Automation Systems Engineer (Siemens)

Biotechnology - Building Automation Systems Engineer (Siemens)

Biotechnology - Building Automation Systems Engineer (Siemens)

PHARMACEUTICAL – SR. CQV ENGINEER

BIOPHARMACEUTICAL – C&Q Manager

Biopharmaceutical CQV SPECIALIST

Biopharmaceutical - CQV Lead/ PROJECT MANAGER

Tired of cold applications?

Responsibilities

Requirements

Full job description

Related keywords

About MMR CONSULTING

About MMR CONSULTING

Similar companies hiring

Tools

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Platform

Clera

Tools

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Platform

Clera