Ankleshwar, Gujarat, India · On-site
JOB TITLE Executive- Quality Control, Pharma JOB PURPOSE Generic To perform QC activities in order to ensure quality of products and services and maintain related documentation to adhere to quality operations and regulat…
Skills: Quality Control, Method Development, Method Validation, cGMP, ISO Standards
Ankleshwar, Gujarat, India · On-site
Job title- Senior Executive - Production, Pharma Education B.Pharm (Bachelor of Pharmacy) , M.Pharm (Master of Pharmacy) Experience 5 to 8 years in pharmaceutical manufacturing (Preferably in Packing ) Key Accountability…
Skills: Pharmaceutical Manufacturing, Packing, SAP, Production Scheduling, Troubleshooting
Ankleshwar, Gujarat, India · On-site
Job Title- Executive Quality Assurance (Pharmaceuticals) Educational requirement B.Pharm or M.Pharm with 1-5 years of experience. Quality Management/Continuous Improvement Line Clearance and shop floor compliance Carry o…
Skills: Quality Assurance, Line Clearance, IPQC, SAP Hana, LIMS
Ankleshwar, Gujarat, India · On-site
Position Title: Executive I - Quality Assurance, Pharma Qualifications & Experience Educational Qualification Bachelor’s or master’s degree in pharmacy, Pharmaceutical Sciences, Life Sciences, or a related discipline. Ex…
Skills: cGMP, GDP, Quality Systems, Batch Documentation, Document Control
Ankleshwar, Gujarat, India · On-site
Position Title: Executive I - Quality Assurance, Pharma Qualifications & Experience Educational Qualification Bachelor’s or master’s degree in pharmacy, Pharmaceutical Sciences, Life Sciences, or a related discipline. Ex…
Skills: cGMP, GDP, Quality Systems, Batch Documentation, Document Control
Ankleshwar, Gujarat, India · On-site
JOB TITLE - Executive : Production, Chemistry JOB PURPOSE Generic Purpose of this job is to co-ordinate and organize API manufacturing activities in shifts adhering to cGMP / HSE norms/ standards with optimum utilization…
Skills: API Manufacturing, cGMP, HSE Standards, SOP Preparation, Equipment Qualification
Ankleshwar, Gujarat, India · On-site
JOB TITLE Senior Executive I - Operations Excellence Specialist REQUIREMENTS Education / Experience Education: Diploma / Graduate/ Post Graduate in Pharmacy Experience: At least 1 to 5 years in the Pharmaceutical plant. …
Skills: Lean Methodology, KPI Reporting, Data Analysis, Process Improvement, Cost Reduction
Ankleshwar, Gujarat, India · On-site
JOB TITLE Assistant Manager I, Quality Compliance JOB PURPOSE Generic Implement Quality Compliance & Regulatory Affairs activities at Ankleshwar site adhering to Zentiva Corporate Quality Policies, Regulatory and HSE gui…
Skills: Quality Compliance, Regulatory Affairs, GMP, CAPA Management, CMC Documentation
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Perform quality control activities including sampling and analysis of raw materials, intermediates, and API to ensure product quality. Manage laboratory documentation, stability studies, and ensure compliance with GMP and HSE regulatory requirements.
Requires a postgraduate degree in Chemistry or Pharmacy with 3-5 years of experience in a cGMP/ISO quality control laboratory. Must possess technical competence in method validation and analytical procedures.
JOB PURPOSE
To perform QC activities in order to ensure quality of products and services and maintain related documentation to adhere to quality operations and regulatory requirements.
All above activity shall be done living Group’s Values and Code of Ethics.
Experience: 3-5 years in a Quality Control/Analysis laboratory in a cGMP/ISO environment, with exposure to method development and validation activities
Generation, managing and archiving Documents including raw data, reports, COA etc as per requirements.
Preparation and implementation of the SOPs in the laboratories system.
Specification preparation and implementing for API raw material and API finished product according to requirement.
Maintaining LIMS data entries
Providing technical support in compiling Annual Product Review.
Analytical method development when required.
Executing on line documentation
Statutory documentation and management
QMS activities
Laboratory ManagementQualification and Validation of instruments/equipment’s
Appropriate training and guidance to the subordinates.
Safety in the laboratory.
Regular housekeeping and upkeep of the work area.
Maintaining adequate inventory of chemicals and reference standards.
Adapting relevant technologies and systems in Quality control.
Laboratory equipment calibration and their maintenance.
Generate up gradation plans as need basis.
Any other activity assigned by the In charge, Quality control
Quality, HSE and ComplianceAdhere to current GMP guidelines
Following ALCOA+++ practices during documentation and related activities
Compliance to local and international HSE norms
Regulatory compliance
ISO 14000 related activities
Regular Pharmacopoeia and regulatory requirement review for compliance
To participate in any regulatory/Customer inspection takes place at the site
Training of self and subordinates on quality and HSE systems
Team memberMember of validation team.
Participating in discussions and giving feedback to Manager, Quality control regarding on-going activities.
Other projectsSupporting new projects (analytical method development (need base), validation, verification)
Laboratory compliance by reviewing documents for completeness
Preventive maintenance, Instrument calibration
New Instrument Qualification
Coordination with OEMs/Service providers for timely services
At Zentiva, we provide health and wellbeing for all generations
Zentiva provides health and wellbeing for all generations, with focus on developing, producing, and delivering high-quality, affordable medicines to more than 100 million people in over 40 countries across Europe and beyond. Zentiva has four manufacturing sites and a broad network of external manufacturing partners. Zentiva employs more than 5,400 unique talents, bonded together by a commitment to the people who depend on our products every day. Visit us at www.zentiva.com. Data protection: It’s not just a checkbox – it’s our commitment! Please visit our Privacy Notice https://www.zentiva.com/gdpr/privacy-notice
Offices: U Kabelovny 529/16, Dolní Měcholupy, Prague 10, 102 00, CZ
There are currently 165 open manufacturing positions in Ankleshwar, India listed on Clera. New openings are added daily as companies post roles.
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