Team Lead - Validation Services

Celltricks Biotech; Bengaluru; Vor Ort; INR 1.200.000 - 1.600.000; Vollzeit

Zusammenfassung

CellTricks is expanding its Validation Services in Bangalore and seeks a Team Lead Validation Services to supervise laboratory validation activities, ensure quality practices, and maintain compliant documentation in line with approved protocols and SOPs.

The role requires a Master’s degree in Microbiology or Biotechnology and 5–8 years of experience in pharma/biopharma contexts, with expertise in GLP, GDP, and laboratory data handling. Immediate joining is preferred.

Qualifikationen

• Master's degree in Microbiology, Biotechnology, or related field.
• 1–3 years of relevant experience in pharmaceutical, biopharma, or contract manufacturing environments.
• Experience in laboratory validation projects and documentation.
• Knowledge of GLP and GDP requirements.
• Hands-on experience with LIMS, ELN, and MS Office tools.

Aufgaben

• Coordinate and execute microbiological and physicochemical studies for validation projects following GLP and GDP where applicable.
• Prepare and review SOPs, protocols, reports, and documentation to ensure compliance.
• Inform Manager of deviations and initiate investigations for protocol or test deviations.
• Support instrument maintenance and inventory management for the department.
• Assist with audits and maintain safety records and MSDS and safe disposal of hazardous waste.

Kenntnisse

Microbiology

Biotechnology

Validation expertise

Ausbildung

Master's degree in Microbiology or Biotechnology

Postgraduate qualification in related field

Tools

LIMS

ELN

MS Office

Jobbeschreibung

Team Lead Validation Services

Location: Bangalore
Experience: 5-8 Years
Qualification: Master s degree in Microbiology, Biotechnology, or a postgraduate qualification in a related field.
Job Type: Full-Time
Joining: Immediate Joiners Preferred

About the Role

CellTricks is expanding its capabilities and is coming up with Validation Services in Bangalore. We are looking for an Team Lead Validation Services to support and execute laboratory validation activities, documentation, quality practices, and compliance in line with approved protocols and SOPs.

Key Responsibilities

• Coordinate and execute microbiological and physicochemical studies for filter validation projects in
  accordance with validation protocols and SOPs, following GLP and considering GDP principles as
  applicable.
• Complete laboratory data forms, interpret results, submit records for approval, and document test results
  in the specified format in accordance with Good Documentation Practices.
• Inform the Manager of deviations related to protocols or test execution, and initiate and complete
  investigations for protocol deviations or out-of-specification results.
• Prepare SOPs, EOPs, qualification protocols and reports, technical reports, and related documentation.
• Support routine maintenance of departmental instruments, oversee third-party maintenance and repairs,
  and assist with inventory management.
• Ensure laboratory compliance with Company Laboratory Quality Assurance and Safety Manuals; prepare
  for and participate in customer and ISO audits.
• Ensure appropriate storage and disposal of hazardous waste; maintain safety records and MSDS;
  coordinate preparation and maintenance of microbial culture strains, culture media, test solutions, and
  reagents as per SOPs or test requirements.
• Perform other laboratory-related tasks as assigned by the Manager.

Key Requirements

• Candidates with experience in bioprocess filtration validation services are highly preferred.
• Master s degree in Microbiology, Biotechnology, or a postgraduate qualification in a related field.
• 1 3 years of relevant experience in pharmaceutical, biopharma, or contract manufacturing environments.
• Knowledge of analytical testing procedures, including microbiological tests such as growth promotion testing and media preparation.
• Awareness of calibration and qualification activities, and knowledge of sterilizing-grade filter applications
  in pharma or biopharma.
• Good understanding of GLP and GDP requirements.
• Knowledge of or hands-on experience with LIMS, ELN, and Microsoft Office tools.

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Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.