Lead Bioanalytical Glp Qa

Year    Bangalore, Karnataka, India

Job Description


JOB DESCRIPTIONDesignation: Deputy ManagerJob Location: BangaloreDepartment: Quality Assurance - GLPAbout SyngeneIncorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene\' s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation.Job Purpose:

  • To Ensure the compliance to Organization for Economic Co-Operation and Development (OECD) principles of Good Laboratory Practices (GLP), Good Clinical Laboratory Practices (GCLP) and ICH GCP
:Key Responsibilities:
  • Receipt and review of general documents/SOPs, MOA, Study Plans and Study Reports
  • Preparation and /or review of SOPs and other documents related to QAU
  • Maintain copies of approved Study Plans, MOA and general documents
  • Review of Method of Analysis and Study plan
  • Performing/scheduling study, facility and process based inspections
  • Perform audit of study raw data & study report
  • Report the observations/findings of inspections to the respective auditee and management in a timely manner
  • Review of electronic data and audit trail for data generated in bioanalysis
  • Review of computerized system documents with respect to OECD 17,21 CFR Part 11 and GAMP
  • Assure that documentation, systems and equipment comply with meeting the requirements of ISO/IEC 17025:2017
  • Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety
  • Attend training on environment, health, and safety (EHS) measures imparted company
  • Prepare the data for quality meetings
  • Review of equipment calibration records, temperature monitoring records of freezers used during study of Archival of inspection reports
  • To prepare, review, and assess CAPA/ cross CAPA requirements
  • To support handling regulatory and client audits/inspection
  • To support the activities of GLP/NABL in preparation/ review and liaising
  • Any other assignments allocated by Quality Assurance Head/ TFM
  • Responsible for maintaining quality culture in the department.
Educational Qualification: Minimum Masters Degree M. Pharm / Masters of Science (Microbiology / Biotechnology/Biochemistry)Technical/functional Skills:
  • Should be well versed with OECD GLP Principles, Bioanalytical Method development and Validation Guidance (Such as USFDA, EMEA, ANVISA), GCLP Guidance, ICH-GCP Guidance
  • Well versed in electronic data audit
  • Good Knowledge on handling the application software
Experience: 10-15 Years\' Experience.Behavioural Skills:
  • Strong commitment towards work, and a high level of dedication, enthusiasm, motivation, and persuasive ability in a team
  • Good speaking-listening-writing skills, attention to details, proactive self-starter
  • Ability to work successfully in a dynamic, ambiguous environment
  • Ability to meet tight deadlines and prioritize workloads
  • Ability to develop new ideas and creative solutions
  • Should able to work in team and flexible for working in shifts
  • Should be a focused employee
Equal Opportunity Employer:It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Syngene International

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Job Detail

  • Job Id
    JD3329906
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Bangalore, Karnataka, India
  • Education
    Not mentioned
  • Experience
    Year