Our Job Offers

Key Responsibilities

• Provide strategic vision and leadership for project teams across all plant locations.
• Lead and supervise projects across multiple plants, ensuring timely and effective execution.
• Manage day-to-day operations in supporting areas while ensuring compliance with applicable standards.
• Lead plant projects with a strong focus on quality, compliance, efficiency, and business objectives.
• Ensure audit readiness and compliance with local and international standards.
• Facilitate and coordinate internal and external audits and ensure timely closure of observations.
• Initiate and supervise cost optimization, operational efficiency, and continuous improvement initiatives in line with the company’s vision.
• Develop team capabilities through effective training, performance management, and succession planning.
• Drive strategic planning and project initiatives aligned with organizational goals and business vision.
• Oversee facility maintenance, renovation, revamping, and development projects.
• Lead equipment induction and facility improvement initiatives while ensuring compliance with pharmaceutical requirements.
• Collaborate with cross-functional stakeholders to ensure successful execution of strategic plant projects.

Requirements

• 15–18 years of experience in Engineering Operations, Project Management, Facility Development, Equipment Induction, and Facility Renovation & Revamping.
• B.E., preferably in Mechanical Engineering; MBA preferred.
• Certification in Project Management and Financial Control will be an added advantage.
• Proficient in MS Office and AutoCAD.
• Strong analytical, communication, technical writing, and interpretation skills.
• Sound knowledge of pharmaceutical regulatory requirements and applicable industry standards.
• Strong leadership, strategic planning, project execution, and stakeholder management capabilities.

If you are a strategic engineering and project leader with extensive pharmaceutical industry experience, we invite you to explore this opportunity with us.

Key Responsibilities

• Plan and execute Computer System Validation (CSV) documentation, including Validation Plans, URS, FS, DS, Risk Assessments, IQ, OQ, PQ Protocols and Validation Summary Reports.
• Validate GxP computerized systems in accordance with GAMP 5, 21 CFR Part 11, EU Annex 11 and applicable regulatory requirements.
• Conduct periodic reviews, system change assessments and revalidation activities.
• Evaluate software changes and upgrades through Change Control.
• Coordinate with IT, software vendors and system owners throughout system implementation and qualification.
• Develop Cleaning Validation Master Plans, protocols and reports.
• Prepare and review URS, DQ, FAT, SAT, IQ, OQ, PQ and qualification reports.
• Qualify pharmaceutical manufacturing facilities, cleanrooms, HVAC systems, purified water systems, compressed air, nitrogen, steam and other critical utilities.
• Collaborate with Production, Engineering, QC, QA, IT and external vendors to ensure successful validation and qualification activities.

Educational Qualifications

• BE/BS – Computer Science / Software Engineering / Computer Systems Engineering
• Pharm-D
• M.Sc. Chemistry / Applied Chemistry

Technical Requirements

• 6–8 years of hands-on experience in Computer System Validation (CSV) within a pharmaceutical or regulated manufacturing environment.
• Strong knowledge of GAMP 5, CSV lifecycle and regulatory expectations.
• Hands-on experience with SAP/ERP, LIMS or other GxP computerized systems.
• Sound knowledge of GAMP 5 categories, URS, Risk Assessment, DQ/IQ/OQ/PQ, 21 CFR Part 11, EU Annex 11 and Data Integrity (ALCOA+).
• Strong problem-solving, communication, coordination and team management skills.
• CSV certification/training will be an added advantage.

Why Join Us?

Be part of a dynamic pharmaceutical environment where you can contribute to regulatory compliance, digital systems validation and qualification of critical pharmaceutical facilities and utilities.

Interested candidates are encouraged to apply and become part of our team.

Key Responsibilities

• Conduct sampling, inspection, and testing of Raw Materials (RM) as per approved procedures.

• Ensure compliance with Good Laboratory Practices (GLP) within the QC laboratory.

• Accurately record, maintain, and archive testing data and documentation.

• Maintain Raw Material retention samples and records in accordance with established procedures.

• Ensure consistency, accuracy, and compliance in all QC activities.

Requirements

• M.Sc. / BS in Chemistry or Pharm-D

• 2–4 years of relevant experience in Quality Control.

• Training in ISO/IEC 17025 and LMS awareness will be preferred.

• Strong attention to detail with a consistent and flexible approach.

• Good documentation and laboratory practices.

Key Responsibilities:

• Support day-to-day production activities under the supervision of senior team members.

• Gain practical exposure to OSD manufacturing processes and production operations.

• Assist in ensuring compliance with GMP and established manufacturing procedures.

• Learn and support routine production documentation and activities.

Qualification: Pharm-D

Experience: Fresh graduates / candidates with up to 6 months of experience are encouraged to apply.

What We’re Looking For:

• Good understanding of GMP and pharmaceutical manufacturing processes.

• Strong willingness to learn and develop technical knowledge.

• Hardworking, proactive, and committed attitude.

• Ability to work effectively under pressure and in shifts, including late sittings when required.

Key Responsibilities:

• Perform sampling, inspection, and testing of raw materials (RM).

• Prepare and maintain SOPs, Specifications, STMs, and related quality records.

• Ensure data integrity, regulatory compliance, and GLP in line with applicable international guidelines.

• Review and update STMs and specifications in accordance with current pharmacopoeial compendia.

• Support continuous improvement of QC laboratory practices and documentation.

Qualifications: M.Sc. / BS in Chemistry or Pharm-D

Experience: 4–6 years of relevant experience in Quality Control within the pharmaceutical industry.

Technical Certification: Training/certification related to ISO/IEC 17025 activities will be preferred.

Key Responsibilities:

• Prepare Product Quality Reviews (PQR) in accordance with applicable standard guidelines and regulatory requirements.

• Perform data integrity reviews of QC laboratories, warehouses, and production floor records.

• Ensure documentation and compliance activities are maintained accurately and in line with established procedures.

Education: Pharm-D / M.Sc. Chemistry

Experience: :1–2 years of relevant experience in QA Documentation, Compliance, Data Integrity, or a related pharmaceutical function.