Ankleshwar, Gujarat, India · On-site
JOB TITLE: Manager Quality Control, Pharmaceuticals REQUIREMENTS Education / Experience M.Sc. or Higher Qualification in Analytical/Organic/Applied/ Pharmaceutical Chemistry.Min. 12- 15 years’ experience in a Quality Con…
Skills: Analytical Ability, Troubleshooting, Coordination, Communication, Leadership
Ankleshwar, Gujarat, India · On-site
JOB TITLE Executive/Sr. Executive, Quality Control, Pharmaceuticals Specific additions- Responsible for LCMS section of Quality control JOB PURPOSE Generic Implement quality control activities for Pharmaceuticals at Ankl…
Skills: Analytical Ability, Troubleshooting, Coordination, Communication, LCMS/MS
Ankleshwar, Gujarat, India · On-site
JOB TITLE- Assistant Manager Quality Control, Pharmaceuticals REQUIREMENTS Education / Experience Post Graduate in Science (Organic or Analytical Chemistry) or B.Pharm/M.Pharm 8-10 years in chemical & instrumental testin…
Skills: Analytical Ability, Troubleshooting, Coordination, Communication, Problem Solving
Ankleshwar, Gujarat, India · On-site
MAIN ACCOUNTABILITIES AND DUTIES Operational skills Operational quality management of a dedicated product portfolio which includes: Quality management of deviation and complaint records and their related CAPAsAssessment …
Skills: Quality Management, GMP Compliance, CAPA Management, Change Control, Auditing
Ankleshwar, Gujarat, India · On-site
JOB TITLE: Executive – Warehouse REQUIREMENTS Education / Experience Graduate in Science / Commerce /Pharmacy and Diploma in Materials Management preferable1 to 3 years of Pharmaceutical Warehouse Technical skills & Comp…
Skills: SAP, Communication, Coordination, Warehouse Management, Inventory Control
Ankleshwar, Gujarat, India · On-site
Perform analysis of raw materials, intermediates, APIs, stability samples, and finished products using HPLC. Operate, calibrate, and maintain HPLC systems as per SOPs. Prepare mobile phases, reagents, standard solutions,…
Skills: HPLC, Analytical Chemistry, Method Validation, GMP, GLP
Ankleshwar, Gujarat, India · On-site
Perform analysis of raw materials, intermediates, APIs, stability samples, and finished products using HPLC. Operate, calibrate, and maintain HPLC systems as per SOPs. Prepare mobile phases, reagents, standard solutions,…
Skills: HPLC, Analytical Method Validation, Method Verification, Method Transfer, GMP
Ankleshwar, Gujarat, India · On-site
JOB TITLE Executive, Quality Control, Chemistry 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 regu…
Skills: Quality Control, Analytical Chemistry, Method Validation, cGMP, ISO Standards
Ankleshwar, Gujarat, India · On-site
Job Posting Title- Executive - Production, Pharma Education B.Pharm (Bachelor of Pharmacy) , M.Pharm (Master of Pharmacy) Experience 1 to 6 years in pharmaceutical manufacturing (Preferably in Packing ) Key Accountabilit…
Skills: Pharmaceutical Manufacturing, SAP, GMP, ISO 14001, Production Scheduling
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
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 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
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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Implement and manage quality control activities for pharmaceuticals, ensuring adherence to regulatory, global quality, and HSE guidelines. Oversee the testing and release of raw materials, intermediates, and finished goods while managing laboratory operations and compliance.
Requires an M.Sc. or higher qualification in Analytical, Organic, Applied, or Pharmaceutical Chemistry. Candidates must have 8-12 years of experience in a QC/Analysis laboratory within a cGMP/ISO environment, specifically in Pharmaceutical or API manufacturing.
JOB PURPOSE
Implement quality control activities for Pharmaceuticals at Ankleshwar adhering to regulatory / global quality guidelines and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet with customers’ requirements, living Group’s Values and Code Ethics.
Planning of timely sampling and analysis and review of raw material, bulk product, intermediates, finished goods, packing material and other samples for Pharmaceuticals.
Performing analysis of Raw Material Samples received from new vendors for Pharmaceuticals.
Planning For analysis of market complaints, Stability, process validation samples and Cleaning Validation of Pharmaceuticals.
Approval / Rejection of Raw Materials, Packaging Components and in process material.
OOS/OOT/Deviation investigations
Review of analytical, chromatographic and computerized data for intermediates, and APIs for Chemistry Ankleshwar.
Timely completion of calibration and calibration of laboratory instrument
Support troubleshooting of QC instruments
LIMS management and support to QC operations
Good Laboratory PracticePlanning for calibration & maintenance of lab. Equipment and assisting for the qualification of laboratory equipment.
Reviewing pharmacopeias for specification preparation.
Preparing SOPs and Formats and Analytical Test Record.
Managing reference standards, working standards, laboratory reagents & chemicals.
Reviewing and observing Retention Samples and maintaining record.
Investigating out of specification results, retesting and review the analysis records.
Maintaining & reviewing laboratory raw data related to testing activity.
Responsible for reviewing the chromatographic data.
ValidationPreparing protocol for Analytical Method validation/Transfer, cleaning validation and performing the validation exercise as per the protocol.
Management of laboratory ConsumablesIdentifying and planning requirement for laboratory consumables and monitoring the stock of chemical, glassware and printed material.
Co ordinationCoordinating with production, QA, QMS and warehouse for analytical activities.
OtherCompliance to HSE Requirements for QC laboratory.
Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situations.
Carrying out any other assignments or projects as per the instruction of the Dept. Head to meet with the organizational objectives and priorities.
Train team members for laboratory related jobs and evaluate for individual development.
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 76 open healthcare positions in Ankleshwar, India listed on Clera. New openings are added daily as companies post roles.
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