Z

Zentiva

Produces branded generic pharmaceuticals in Europe

Executive, Quality Control, Chemistry

Full-TimeUpdated on 10/23/2026
No salary listed
Mid, Senior
Master's
India
In PersonWorkplace in Ankleshwar, India.
Biology & BiotechRegulatory & Quality (Life Sciences)

About the job

Requirements
  • Postgraduate qualification in Chemistry or Pharmacy.
  • Three to five years of experience in a quality control or analysis laboratory in a cGMP or ISO environment, with exposure to method development and validation activities.
  • Technical competence.
  • Leadership skills.
  • Analytical ability.
  • Planning ability.
  • Communication skills.
  • Problem-solving ability.
  • Team-building skills.
Responsibilities
  • Perform quality control activities and maintain related documentation to support product and service quality, quality operations, and regulatory requirements.
  • Sample, analyze, and ascertain the quality of raw materials, packaging materials, intermediates, in-process samples, and active pharmaceutical ingredients for Chemistry Ankleshwar.
  • Test method-validation samples, process-validation samples, and cleaning-validation samples.
  • Analyze and document active pharmaceutical ingredient finished-product stability studies according to the stability study protocol.
  • Coordinate with Production, Stores, and QCAA on approval or rejection of raw materials and finished products.
  • Validate and verify analytical procedures as required.
  • Report out-of-specification and out-of-trend results and deviations.
  • Maintain retained samples according to standard procedures.
  • Assist with customer complaint investigations.
  • Test new samples for vendor approval.
  • Train subordinates and suggest corrective actions and preventive actions to upgrade the quality system.
  • Maintain and manage stability samples; dispose of waste according to approved procedures; reduce waste generation and manage effluent.
  • Coordinate with the microbiology laboratory for microbial analysis of pharmaceutical products and utilities.
  • Generate, manage, and archive documents, including raw data, reports, and certificates of analysis.
  • Prepare and implement laboratory system standard operating procedures.
  • Prepare and implement specifications for active pharmaceutical ingredient raw materials and finished products.
  • Maintain Laboratory Information Management System data entries.
  • Provide technical support for compiling the Annual Product Review.
  • Develop analytical methods when required and execute online documentation and statutory documentation management.
  • Perform quality management system activities.
  • Qualify and validate instruments and equipment; train and guide subordinates; maintain laboratory safety and housekeeping.
  • Maintain inventory of chemicals and reference standards and adopt relevant quality-control technologies and systems.
  • Calibrate and maintain laboratory equipment and generate upgrade plans as needed.
  • Perform other activities assigned by the Quality Control In-charge.
  • Adhere to current good manufacturing practice guidelines and ALCOA+++ documentation practices, and comply with local and international health, safety, and environmental norms and regulatory requirements.
  • Perform ISO 14000-related activities and review pharmacopoeia and regulatory requirements for compliance.
  • Participate in regulatory and customer inspections at the site.
  • Train self and subordinates on quality and health, safety, and environmental systems.
  • Participate as a member of the validation team and provide feedback to the Quality Control Manager on ongoing activities.
  • Support new projects involving analytical method development, validation, and verification.
  • Review documents for completeness to support laboratory compliance.
  • Perform preventive maintenance, instrument calibration, and new instrument qualification.
  • Coordinate with original equipment manufacturers and service providers to ensure timely service.

About the company

Zentiva makes branded generic medicines in Europe. Its products are off-patent drugs sold under Zentiva brands with the same active ingredients and safety as the originals, usually at lower cost. The company distinguishes itself through a long history and growth by acquisitions to expand across Europe, especially after becoming independent under private equity. Its goal is to be a leading European branded generics platform by widening its product lineup and geographic reach.

Company Size

1,001-5,000

Company Stage

Acquired

Total Funding

N/A

Headquarters

Prague, Czechia

Founded

2003

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Simplify Jobs

Simplify's Take

What believers are saying

  • The December 1, 2025 biosimilar launch opens higher-margin, less commoditized European demand.
  • GTCR's April 2026 buyout likely funds portfolio expansion and manufacturing investment.
  • Zentiva's manufacturing footprint in Czechia, Romania, and India supports supply security and scale.

What critics are saying

  • MHRA recalled Fingolimod Zentiva on August 20, 2026 for metal-particle contamination.
  • Zentiva's February and April 2026 UWWTD fights signal looming cost pressure across Europe.
  • Biogen won Hamburg damages against Zentiva in 2026, exposing patent-litigation and payout risk.

What makes Zentiva unique

  • Zentiva serves 100 million people across 40 countries with four manufacturing sites.
  • Its December 2025 biosimilar launch marked entry into biologics, beyond classic generics.
  • GTCR closed the April 9, 2026 acquisition, backing growth under management continuity.

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Benefits

  • Health Insurance
  • Life Insurance
  • Paid Vacation
  • Paid Sick Leave
  • Meal Benefits
  • Relocation Assistance
  • Flexible Work Hours
  • Performance Bonus
  • Training Programs
  • Professional Development Budget
  • Company Social Events

Growth & Insights and Company News

6 month growth

0%

1 year growth

0%

2 year growth

8%
Dispex
Aug 24th, 2026
Class 2 Medicines Recall: Zentiva Pharma UK Limited, Fingolimod Zentiva 0.5 mg Capsules, EL(26)A/37.

Class 2 Medicines Recall: Zentiva Pharma UK Limited, Fingolimod Zentiva 0.5 mg Capsules, EL(26)A/37. Zentiva UK Pharma Limited are recalling one batch of Fingolimod Zentiva 0.5 mg Capsules (BN 4L01372H) as a precautionary measure due to a potential risk of contamination with metal particles DMRC reference number. DMRC - 39754868 Marketing authorisation holder. Zentiva Pharma UK Limited Medicine details. Fingolimod Zentiva 0.5 mg Capsules. PL: 17780/0858 Active Ingredient: Fingolimod SNOMED code: 40459211000001106 GTIN: 8594739260931 Affected lot batch numbers. | Batch No. Expiry Date | Pack Size | First Distributed | | 4L01372H | 11/2027 | 28 | 28 January 2025 | Background. Zentiva UK Pharma Limited are recalling one batch of Fingolimod Zentiva 0.5 mg Capsules (BN 4L01372H) as a precautionary measure due to a potential risk of contamination with metal particles. The particles, if present, are known to be small and pose a low risk to the safety or efficacy of the tablets. No reports have been received to date, the particles were identified during shelf-life testing. Advice for healthcare professionals: Stop supplying the affected batch. Quarantine all remaining stock and return it to your supplier using your supplier's approved process. Advice for patients: If patients have the affected batch they should contact their pharmacy in the first instance. Do not stop taking your medication without speaking to your healthcare professional first. The particles, if present, are known to be small and pose a low risk to the safety of the product. Patients with this batch are not considered at risk and no reports of harm have been reported for this batch of capsules. Patients who experience adverse reactions or have any questions about the medication should seek medical attention. Any suspected adverse reactions should also be reported via the MHRA Yellow Card scheme. Additional information: For all medical information enquiries and information on this product, please email [email protected], or telephone 0800 090 2408. Recipients of this Medicines Recall should bring it to the attention of relevant contacts by copy of this notice. NHS regional teams are asked to forward this to community pharmacists and dispensing general practitioners for information. Yours faithfully Defective Medicines Report Centre 10 South Colonnade Canary Wharf Telephone +44 (0)20 3080 6574

V3 Healthcare
Dec 2nd, 2025
Demonstrating accountability: Zentiva receives prestigious ESG Transparency Award 2025

Demonstrating accountability: Zentiva receives prestigious ESG Transparency Award 2025. PRAGUE, Nov. 28, 2025 /PRNewswire/ - Zentiva, a leading European generics pharmaceutical company, has received the esteemed ESG Transparency Award 2025 by the EUPD Group. This award recognises companies that excel in clarity, structure and transparency in their Environmental, Social and Governance (ESG) reporting. The awards were presented at the ESG Summit 2025, as part of the European Sustainability Week 2025, hosted by the EUPD Group. The recognition is a testament to the efforts of industry leaders who have embedded sustainability in their business strategy and communicate it transparently according to relevant standards. Zentiva received recognition at the Excellence Level of the ESG Transparency Award 2025 for its high degree of clarity, accessibility and transparency in sustainability reporting. The Excellence Level distinction places Zentiva among the top organisations in Europe in terms of transparent reporting of its ESG disclosures. The company excelled in the presentation of a well-structured and strategically grounded sustainability approach that incorporates current European requirements into governance and reporting processes. Furthermore, the disclosure of climate related information, including the use of renewable electricity at European production sites and its integration into a broader long term climate strategy reached a high level of transparency. In addition, Zentiva offered a full calculation of the indirect carbon footprint with externally reviewed methodology to strengthen data integrity and clearly explained its governance structures, highlighting the role of the Audit Committee in approving sustainability related plans. These results underline the determination of Zentiva to strive to drive positive change for society and the environment. Steffen Klink, COO of the EUPD Group commented: "We proudly congratulate Zentiva on its exceptional commitment to transparent ESG communication, clearly demonstrating accountability by publicly detailing material impacts, risks, and opportunities across key environmental, social, and governance areas. This dedication to holistic performance, including ambitious decarbonization targets and robust global policies on ethical conduct and responsible sourcing, sets a definitive benchmark for industry excellence." Ines Windisch, Head of Corporate Affairs & Sustainability at Zentiva, commented: "We are truly proud to receive this award for our sustainability reporting. It acknowledges a journey that is far more than just compliance - it is about learning, testing, piloting, and acting with courage and transparency. At Zentiva we understand small steps can create a big impact, and we must act today for a sustainable tomorrow. Sustainability is not just a responsibility; it is an opportunity for people and partners to create a lasting positive impact for future generations. This award is a milestone that inspires us to keep moving forward." About Zentiva 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 30 countries across Europe and beyond. Zentiva has four wholly-owned manufacturing sites and a broad network of external manufacturing partners to ensure supply security. Zentiva employs more than 5,000 unique talents, bonded together by a commitment to the people who depend on its medicines every day. Visit Healthcare at www.zentiva.com About the ESG Transparency Award The ESG TRANSPARENCY AWARD honours European organisations that have already anchored forward-looking sustainability concepts in their company and communicate these transparently in the form of a sustainability report. These pioneers serve as role models because they change the world and prove that profitability and sustainability are not opposites, but successful strategies for a future worth living. The EUPD Group has developed the ESG Transparency Evaluation Standard to objectively assess transparency, accountability and structural quality of ESG reporting. It draws on the most relevant European and international guidelines of sustainability reporting and serves as the methodical basis of the ESG Transparency Award. www.esg-transparency-award.de/en/ SOURCE Zentiva

Tekedia
Sep 12th, 2025
GTCR Clinches $4.8bn Deal to Acquire Zentiva from Advent International

India's Economic Times reported last month that Aurobindo Pharma, one of India's largest generics manufacturers, had been leading the race to acquire Zentiva with an offer reportedly valued at up to $5.5 billion.

Czech News Center
Sep 11th, 2025
Zentiva acquired by GTCR for €4.1B

American investment firm GTCR is acquiring Czech drug manufacturer Zentiva from Advent International for €4.1 billion, including debts, as reported by the Financial Times. This sale marks a significant increase from the €1.9 billion Advent paid in 2018. The transaction, resulting from a bidding process, highlights growing investor interest in stable pharmaceutical companies in the region. The deal is expected to be officially announced soon.

The Economic Times
Aug 19th, 2025
Aurobindo Pharma nears $5.5B Zentiva acquisition

Aurobindo Pharma is set to acquire Prague-based Zentiva for $5-5.5 billion, marking the largest-ever acquisition by an Indian pharma company. Competing with US firm GTCR, Aurobindo has secured a $4.75 billion credit line from MUFG, with the remaining $800 million from internal funds. This acquisition will enhance Aurobindo's European presence, especially in Eastern Europe. Zentiva's 2024 revenues are projected at €1.7 billion with an EBITDA of €400 million.