Zentiva

Produces branded generic pharmaceuticals in Europe

Executive Quality Control - Pharmaceuticals

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours

Full-timeAnkleshwar, Gujarat, IndiaNo salary listedIn-person

About the Job

Requirements

Postgraduate qualification in Science, specializing in Organic Chemistry or Analytical Chemistry.
One to four years of experience in a pharmaceutical company.
Analytical ability.
Troubleshooting ability.
Coordination skills.
Communication skills.
Accountability, authenticity, collaboration, courage, and trust.

Responsibilities

Implement quality control activities for pharmaceuticals at Ankleshwar in accordance with regulatory and global quality directives and health, safety, and environmental guidelines, using resources effectively to ensure consistent product quality that meets customer requirements and complies with organizational values and the Code of Ethics.
Perform timely analysis of raw materials, bulk products, intermediates, finished goods, and other pharmaceutical samples.
Analyze market complaints, stability samples, process validation samples, and pharmaceutical cleaning validation samples.
Calibrate and maintain laboratory equipment, and assist with laboratory equipment qualification.
Review pharmacopeias to prepare specifications.
Prepare standard operating procedures, formats, and analytical test records.
Manage reference standards, working standards, laboratory reagents, and chemicals.
Arrange and observe control samples and maintain their records.
Participate in investigations of out-of-specification results, retesting, and review of analysis records.
Maintain and review laboratory raw data related to testing activities.
Prepare protocols for analytical method validation and cleaning validation, and perform validation according to the protocols.
Identify and plan laboratory consumable requirements, and monitor stocks of chemicals, spares, glassware, and printed materials.
Coordinate analytical activities with production and warehouse teams.
Comply with health, safety, and environmental requirements for the quality control laboratory.
Identify and correct unsafe conditions or behaviors, and promptly report other potentially hazardous situations.
Carry out other assignments or projects as instructed by the department head to meet organizational objectives and priorities.

JOB TITLE

Executive Quality Control, Pharmaceuticals

REQUIREMENTS

Education / Experience

Post Graduate in Science (Organic or Analytical Chemistry )

1-4years in a Pharmaceutical Company.

Technical skills &

Competencies / Language

Analytical ability

Trouble shootings

Co ordination

Communication

Behavioural Competencies

(LEAD and others)

Accountability, Authenticity, Collaboration, Courage and Trust

JOB PURPOSE

Generic

Implement quality control activities for Pharmaceuticals at Ankleshwar adhering to regulatory / global quality Directives 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 of Ethics.

KEY ACCOUNTABILITIES

Testing

Performing timely analysis of raw material, bulk product, intermediates, finished goods and other samples for Pharmaceuticals.

Performing analysis of market complaints, Stability, process validation samples,Cleaning Validation of Pharmaceuticals.

Good Laboratory Practice

Performing calibration & maintenanceof 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.

Arranging and observing Control Samples and maintaining record.

Participating in Investigation of out of specification results, retesting and review the analysis records.

Maintaining & reviewing laboratory raw data related to testing activity.

Validation

Preparing protocol for Analytical Method validation, cleaning validation and performing the validation exercise as per the protocol.

Management of laboratory Consumables

Identifying and planning requirement for laboratory consumables and monitoring the stock of chemical, spares, glassware and printed material.

Co ordination

Coordinating with production, and warehouse for analytical activities.

Other

Compliance 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.

About the Company

Zentiva

Produces branded generic pharmaceuticals in Europe

Zentiva makes branded generic medicines for European markets. Its products are off-patent drugs reformulated and marketed under Zentiva’s brands, delivering the same active ingredients and dosage as original medicines at lower prices. It differentiates itself through a long history as an independent platform under private equity, with a growth strategy built on acquiring brands to expand its European footprint. The goal is to become a leading European branded generics platform and improve access to affordable medicines across its markets.

Company size: 1,001-5,000
Company stage: IPO
Headquarters: Prague, Czechia
Founded: 2003

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