Manager Microbiology

SUN PHARMA; Dhar; On-site; INR 1,800,000 - 3,000,000; Full time

Job summary

Sun Pharma in Pithampur is seeking a Manager Microbiology to lead microbiology quality activities and ensure GMP compliance across the Global Quality and Compliance unit.

You will coordinate equipment qualification, support risk assessments, and manage aseptic process verification, with emphasis on regulatory standards (USP/EP).

The role requires 12+ years in pharma microbiology, MSc in Microbiology, and the ability to collaborate across Production, QA and Engineering.

Qualifications

• MSc in Microbiology or equivalent.
• 12+ years of microbiology experience in pharma QA/QC.
• Experience with GMP, regulatory audits.

Responsibilities

• Coordinate procurement, evaluation, installation and qualification of equipment.
• Lead design reviews, risk assessments, and GMP reviews from microbiology view.
• Support qualification of HVAC, cleanrooms, biosafety cabinets, autoclaves, incubators, utilities.
• Prepare SOPs, specs, test procedures, validation protocols and summaries.
• Handle Change Control, Deviation, CAPA, OOS/OOT.
• Conduct contamination-control risk assessments and CCS implementation.
• Support microbiological method verification/validation per pharmacopoeia.

Skills

GMP knowledge

Risk assessment

QA documentation

Cross-functional coordination

Microbiology testing

Environmental monitoring

Education

MSc in Microbiology

Tools

Biosafety cabinets/LAFs

Autoclaves

Incubators

HVAC systems

Cleanrooms

Job description

Responsibilities

At Sun Pharma, we commit to helping you

Job Title

Manager Microbiology

Business Unit

Global Quality and Compliance

Job Grade

G10

Location

Pithampur

Responsibilities

At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.

Are You Ready to Create Your Own Sunshine?

As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”

• Coordinate equipment procurement, technical evaluation, installation and qualification.
• Participate in design review, risk assessment, constructability review and GMP review from a Microbiological perspective.
• Participate in DQ, FAT, SAT, IQ, OQ and PQ activities for systems impacting microbiological quality.
• Support qualification of: HVAC systems, Cleanrooms, Biosafety cabinets/LAFs, Autoclaves, Incubators, Utilities
• Support qualification of: HVAC systems, Cleanrooms, Biosafety cabinets/LAFs, Autoclaves, Incubators, Utilities
• Support qualification of: HVAC systems, Cleanrooms, Biosafety cabinets/LAFs, Autoclaves, Incubators, Utilities
• Prepare SOPs, Specifications, Standard Test procedures, QRM, Validation protocols & summary reports.
• Handling of Change Control, Deviation, CAPA, OOS/OOT.
• Perform/participate in contamination-control risk assessments & implementation of CCS.
• Support microbiological method verification/validation. Establish microbiological testing procedures based on applicable pharmacopoeia and regulatory requirements.

Microbial enumeration

Microbiological Assay

Sterility testing

Bacterial endotoxin testing

Bioburden testing

Water microbiology

Environmental monitoring

• Establish microbiological requirements for cleaning and disinfection programs & develop and execute disinfectant efficacy studies. Support cleaning validation with microbiological risk assessment
• Provide Microbiological SME support for aseptic process design.
• Develop Microbiology requirements for Aseptic Process Simulation (APS)/Media Fill .
• Participate in media fill protocol preparation, execution and assessment
• Ensure documentation completeness, accuracy, and compliance with data integrity principles.
• Coordinate with cross-functional teams (Production, QA, Engineering) to align with project timelines.
• Monitoring of training of laboratory team as per job role
• Strong knowledge of USP, EP, JP, PICS, PDA, WHO Microbiological requirements.

EU GMP Annex 1

21 CFR Part 210 & 211

Data Integrity requirements

ISO 14644

PDA Technical Reports

Sterility Assurance Principles

Environmental Monitoring Programs

Contamination Control Strategy (CCS)

Travel Estimate

NA

Job Requirements

Education Qualification

M.Sc. in Microbiology.

Experience

Tenure : 12+ Years

Your Success Matters to Us

At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!

Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).