Maple Grove, Minnesota, United States · On-site
$192k–$260k/yr
About Bora Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in formulation development, clinical and commercial manufacturing, and packaging of compl…
Skills: Quality Management System, CGMP/GxP Compliance, Regulatory Inspections, Quality Assurance, Quality Control
Maple Grove, Minnesota, United States · Hybrid
$107k–$203k/yr
Additional Location(s): US-MN-Maple Grove; US-MN-Arden Hills Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all …
Skills: Employee Engagement, Content Strategy, Internal Communications, Editorial Management, Storytelling
Maple Grove, Minnesota, United States · Hybrid
$148k–$281k/yr
Additional Location(s): US-MN-Arden Hills; US-MA-Marlborough; US-MN-Maple Grove Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportun…
Skills: Global Trade Compliance, Customs Valuation, HTS Classification, ECCN Classification, Export Controls
Edina, Minnesota, United States · On-site
$112k–$171k/yr
The Nurse Practitioner is responsible for providing primary care services, including assessing, diagnosing, prescribing, treating, and educating patients. Works closely with physicians and other clinicians in a team appr…
Skills: Patient Assessment, Diagnosis, Prescribing Medications, Patient Education, Women's Health
Maple Grove, Minnesota, United States · On-site
ABOUT VEG In 2014, VEG was born with a mission to help people and their pets when they need it most. This meant challenging the status quo and fixing everything that was wrong with the ER experience. Since then, we’ve ex…
Skills: Triage, Nursing Care, Diagnostics, Catheter Placement, Oxygen Support
Maple Grove, Minnesota, United States · On-site
ABOUT VEG In 2014, VEG was born with a mission to help people and their pets when they need it most. This meant challenging the status quo and fixing everything that was wrong with the ER experience. Since then, we’ve ex…
Skills: Triage, Nursing Care, Diagnostics, Bloodwork, Imaging
Maple Grove, Minnesota, United States · On-site
ABOUT VEG In 2014, VEG was born with a mission to help people and their pets when they need it most. This meant challenging the status quo and fixing everything that was wrong with the ER experience. Since then, we’ve ex…
Skills: Triage, Anesthesia Monitoring, Critical Care Nursing, IV Placement, CRIs
Maple Grove, Minnesota, United States · On-site
$50/hr–$65/hr
Job Title: Speech Language Pathologist Pay Range: $50-$65/hour Job Description: 26/27 School Year | $50-$65/hour | Full-Time | Maple Grove, MN | State SLP and PEL License Required + Clinical Fellows are welcome to apply!…
Skills: Speech and Language Therapy, Student Assessment, Treatment Planning, IEP Development, Interdisciplinary Collaboration
Maple Grove, Minnesota, United States · On-site
$20/hr–$23/hr
The Wealshire is a family oriented assisted living care facility that specializes in dementia/Alzheimer’s care. We are currently looking to employ Part Time Housekeeping Aides for our Medina Community. The Wealshire prid…
Skills: Housekeeping, Laundry Management, Organization, Detail Orientation, Time Management
Maple Grove, Minnesota, United States · On-site
$22/hr–$34/hr
Posting Date 07/15/2026 15655 Grove Cir N, Maple Grove, Minnesota, 55369-4489, United States of America Patient Care Technician - PRN - Certified Clinical Hemodialysis Technician CCHT is REQUIRED DaVita Skilled Nursing D…
Skills: Hemodialysis, Patient Care, Patient Monitoring, Machine Setup, Critical Thinking
Maple Grove, Minnesota, United States · On-site
When you work at Havenwood of Maple Grove, you have a front-row seat to the amazing life stories of the wisest people on earth. What’s more, you are part of an extraordinary company – one that’s investing in the future o…
Skills: Personal Care, Vital Signs Monitoring, Patient Grooming, Incontinent Care, Meal Assistance
Maple Grove, Minnesota, United States · On-site
$120k–$147k/yr
Position Details Schedule: Full-Time, salaried, exempt position (open to a 0.8 FTE, 0.9 FTE or 1.0 FTE) Location: Maple Grove - MNGI Digestive Health Salary Range: Starting range $120,000 - $147,000 (Where an applicant m…
Skills: Compassionate Patient Care, Active Listening, Problem Solving, Prioritization, Critical Thinking
Maple Grove, Minnesota, United States · Hybrid
$97k–$184k/yr
Additional Location(s): N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in t…
Skills: Curriculum Development, Clinical Training, IVUS, Intravascular Physiology, CTOs
Maple Grove, Minnesota, United States · On-site
$42k–$52k/yr
Our Mission: Honoring People Our Values: Integrity, Compassion, Curiosity, and Helpfulness The Medical Records Specialist is responsible for various medical records and administrative functions for the parent and branch …
Skills: Medical Records Management, Compliance Monitoring, Electronic Medical Records, Provider Management, Time Management
Maple Grove, Minnesota, United States · On-site
$20/hr–$22/hr
POSITION: Part-Time Cook COMPANY: Suite Living Senior Care LOCATION: Maple Grove, MN TYPE: Part Time SHIFT: Full Day Weekends and Half Day Weekdays PAY RANGE: $20-22/hr SUMMARY: Suite Living Senior Care is seeking a Part…
Skills: Cooking, Kitchen Clean-up, Meal Preparation, Dependability, Adaptability
Maple Grove, Minnesota, United States · On-site
About Upsher Smith At Upsher-Smith, we strive to improve the health and lives of patients by manufacturing and marketing brand and generic pharmaceutical products across multiple therapeutic areas. Our work is always bac…
Skills: Supply Planning, SAP, Inventory Management, Contract Manufacturing Management, S&OP/IBP
Maple Grove, Minnesota, United States · On-site
$25/hr–$27/hr
** $25-27 per hour ** 11:00am - 8:00pm, Every other weekend required When you work at Havenwood of Maple Grove you have a front-row seat to the amazing life stories of the wisest people on earth. What’s more, you are par…
Skills: Production Cooking, Food Quality Control, Sanitation Standards, Menu Cycle Implementation, Dietary Compliance
Maple Grove, Minnesota, United States · On-site
$16/hr–$18/hr
When you work at Havenwood of Maple Grove, you have a front-row seat to the amazing life stories of the wisest people on earth. What’s more, you are part of an extraordinary company – one that’s investing in the future o…
Skills: Food Service, Customer Service, Serving Etiquette, Sanitation, Organization
Maple Grove, Minnesota, United States · Hybrid
$126k–$239k/yr
Additional Location(s): N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in t…
Skills: Data Product Management, Snowflake, Commercial Analytics, Team Leadership, Stakeholder Engagement
Maple Grove, Minnesota, United States · On-site
$80k–$100k/yr
We're Hiring: Manufacturing Engineer II Location: Maple Grove, MN Company: Peli BioThermal About Us: Peli BioThermal offers the widest range of temperature-controlled packaging and service solutions to the global life sc…
Skills: Equipment Validation, Process Development, Lean Manufacturing, Root Cause Analysis, IQ/OQ/PQ
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The Site Head of Quality is responsible for developing and overseeing a comprehensive Quality Management strategy to ensure products are safe, effective, and compliant with global regulatory standards. This role leads the Quality organization, manages regulatory inspections, and partners with site leadership to foster a culture of accountability and continuous improvement.
Candidates must have over 10 years of experience in GMP-regulated pharmaceutical manufacturing, including at least 5 years in senior leadership. Strong knowledge of global regulatory requirements (FDA, EMA, ICH) and experience in a CDMO environment are highly preferred.
Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in formulation development, clinical and commercial manufacturing, and packaging of complex oral solid dose, liquid, semi-solid, biologics, and sterile injectable pharmaceutical products. From our world-class sites in North America and Asia, we deliver drug products with unparalleled quality to more than 100 markets around the world. Bora’s teams, technologies, and facilities work seamlessly together to enable our clients to deliver much-needed therapeutics to patients worldwide. At Bora Pharmaceuticals, we see it as our mission, our duty, our responsibility, to make our success and our customer’s success more certain.
Reporting to the VP, Regional Head of Quality, the BPI Site Head of Quality is responsible for developing, implementing, and overseeing a comprehensive Quality Management strategy aligned with corporate policies, client expectations, and global regulatory requirements. This role ensures products from development through commercialization are safe, effective, and fully compliant with applicable CGMP/GxP standards. As a key member of the site leadership team, the Director/Sr. Director of Quality provides strategic and operational leadership for the Quality organization, which includes Quality Assurance and Quality Control. The role partners cross-functionally with all departments to foster a strong culture of quality, accountability, collaboration, and continuous improvement while ensuring regulatory compliance and client satisfaction.
The Director/Sr. Director also directs day-to-day quality operations, drives operational excellence and process optimization, supports execution of strategic and tactical initiatives, and ensures timely resolution of quality and compliance issues to maintain business performance and inspection readiness.
Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions.
Provide strategic leadership and overall accountability for the site Quality Management System (QMS), ensuring compliance with global policies, procedures, CGMP/GxP standards, and applicable regulatory requirements across the U.S. and international markets.
Partner with the Site Leadership Team (SLT) to strengthen and sustain a proactive culture of quality, escalating significant compliance risks and driving timely, effective resolution of quality issues.
Lead and oversee regulatory inspections and audits, ensuring inspection readiness, effective agency interactions, and timely, compliant responses to observations.
Direct all core Quality functions, including batch record review, material and product disposition, deviations and change control, document control, QC, QA oversight of all GMP functions including validation, quality engineering, and facility activities.
Provide leadership to ensure uninterrupted support for successful product transfers through robust quality oversight and operational excellence.
Serve as the senior Quality leader supporting development initiatives and phased clinical programs, ensuring appropriate compliance throughout product development activities.
Lead the Quality organization in achieving operational and strategic objectives, including budget planning and management, workforce planning, project execution, and organizational effectiveness.
Build, mentor, and develop a high-performing Quality organization that operates as a trusted, collaborative business partner, while driving talent development, succession planning, and employee growth.
Establish clear, consistent, and effective communication across the Quality organization and with cross-functional stakeholders to ensure alignment on priorities, risks, and business objectives.
Perform additional responsibilities and strategic initiatives as assigned
The above statements are intended to describe the nature of work performed by those in this job and are not an exhaustive list of all duties. Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time which reflects management’s assignment of essential functions.
10+ years of progressive experience within GMP-regulated pharmaceutical and/or combination drug-device manufacturing environments.
Strong working knowledge of global regulatory requirements and quality standards, including US FDA, EMA, PIC/S, and ICH guidelines.
5+ years of senior leadership experience driving Quality strategy, operational excellence, compliance initiatives, and continuous improvement programs.
Proven ability to build and sustain a transparent, collaborative, and quality-focused culture that promotes accountability, engagement, and operational performance.
Demonstrated experience leading cross-functional teams and influencing organizational change within complex regulated environments.
Prior experience within a CDMO environment is strongly preferred.
Other Knowledge, Skills and Abilities
Strong knowledge of pharmaceutical manufacturing operations, including Oral Solid Dose (OSD) processes and associated quality requirements.
Demonstrated success in leading organizations through sound decision-making, strategic problem-solving, and effective communication at all levels of the business.
Proven track record of successfully managing and leading regulatory inspections, audits, and remediation activities with global health authorities.
Exceptional written and verbal communication skills, with the ability to influence stakeholders and communicate complex quality and compliance matters clearly and effectively.
Proven ability to lead, mentor, and support teams through crisis management, organizational transformation, cultural change, and business growth initiatives.
Highly adaptable and resilient, with the ability to perform effectively in fast-paced, high-pressure environments while maintaining focus on priorities and outcomes.
Strong leadership capability with a demonstrated ability to empower teams, identify high-potential talent, and drive employee development and succession planning.
Results-oriented leader with strong analytical and problem-solving skills focused on continuous improvement and operational excellence.
Skilled at building trusted relationships and collaborating effectively with cross-functional peers, senior leadership, clients, and regulatory agencies.
We offer a comprehensive benefits package designed to support our employees’ wellbeing, including:
Competitive salary and performance-based incentives
Comprehensive health coverage including medical, dental, and vision insurance
Retirement savings plans with employer matching contributions
Paid time off
Professional development opportunities
Employee wellness programs and resources
Employee Assistance Program and Mental Health Resources
At Bora, our values guide everything we do — from how we solve challenges to how we support our people. We lead with a solutions-first mindset, strive to do the right thing, stay proactive, and above all, respect everyone.
Bora Pharmaceuticals is committed to providing equal employment opportunity to all applicants and employees according to all applicable equal opportunity and affirmative action laws, directives and regulations of federal, state and local governing bodies and agencies. In keeping with this commitment, Bora Pharmaceuticals will recruit, hire, train and promote persons in all job titles, without regard to race, color, creed, religion, sex (including factors related to pregnancy or child birth), national origin, age, marital status, familial status, disability, sexual orientation, gender identity status with regard to public assistance, employment status, local human rights commission activity, status as a protected veteran, genetic information, atypical hereditary cellular or blood trait, or any other protected category.
A premier international CDMO, making success more certain.
Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in complex oral solid dose, liquids, semi-solids, opthalmics, biologics, and sterile injectable products. We provide early phase clinical through to commercial manufacturing with full packaging capabilities to biopharma companies worldwide. Bora owns and operates in ten state-of-the-art CGMP manufacturing facilities across Asia and North America – delivering to more than 100 markets around the world. Our sites have the highest international standards for manufacturing, packaging, R&D and analytical testing. As a future focused CDMO, we know better than most that our own success is shaped by our partners victories. That's why, when you choose Bora - we make success more certain by following Bora’s 5Ps – Promises, Partnerships, Pride, People, and Progress. These 5 principles are Bora’s Pledge to our customers. Follow us to find out more and keep up to date with Bora Pharmaceuticals.
Offices: o. 2號, Alley 36, Lane 26, Ruiguang Road, Neihu District, Taipei, Taiwan 114, TW · No. 1, Kedong 3rd Road, Hsinchu Science Park, Zhunan, Miaoli 35053, TW · 7333 Mississauga Rd, Mississauga, Ontario L5N 6L4, CA · No. 54 Gongye West Road, Guantian District, Tainan City, 720, TW · No. 80, Sec. 1, Channg'an Rd., Luzhu Dist., Taoyuan City, 338, TW
There are currently 235 open healthcare positions in Maple Grove, MN listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include Boston Scientific, Anteris Technologies, Children's Minnesota, Fairview Health Services, Teleflex, among others. Browse the listings above to see every active employer.
Yes — 39 of the 235 open healthcare positions offer remote or hybrid work (8 remote, 31 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
