Johnson & Johnson Officer Quality Control Vacancy – Apply Online

Johnson & Johnson Officer Quality Control Vacancy – Apply Online

Johnson & Johnson chemistry job opening 2021. Msc Chemistry job opening 2021, chemistry job opening 2021. Msc jobs 2021. Johnson & Johnson announces job openings for chemistry candidates. Chemistry job opening 2021. Chemistry job opening 2201. Check out all the details on the same below:

Primary Location India-Maharashtra-Greater Mumbai-

Organization Johnson & Johnson Private Limited (8080)

Job Function Quality

Requisition ID 2105935237W

Job Title: Officer Quality Control

Requirements & Qualifications

Qualifications requirement, a Master Degree in Chemistry, or related science discipline with 3-5 years of related work experience in Pharma, Healthcare Industry. Knowledge of cGMPs and related compliance regulations and guidelines is required. CTS requirement is Good to have.

Minimum Skills Requirements

• Must have the ability and skill to perform detailed job requirements noted above competently, safely, and proficiently.
• A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.
  Must have excellent organizational, verbal communication, and technical documentation skills.
• Good computer skills.
• Knowledge of safe laboratory practices, proper knowledge of handling chemicals and samples.
• Must be a team player with high integrity and concern for the quality of Company products, services, and staff members.

Job Description Summary for Officer Quality & Compliance

The QC Chemist conducts a quantitative and qualitative analysis of regulated products according to FDA, cGMP, and Johnson & Johnson Pvt. Ltd. Standard Operating Procedures. Duties will include analysis of Cosmetic products through compendial methods and specific test protocols. In addition, the QC Chemist shall be involved in plant interactions, system improvements, and validation activities (Instrument and Method).

Primary Duties And Responsibilities

• To ensure compliance of Good Laboratory Practices (GLP) & Good Documentation Practices (GDP) in Quality Control Analytical Laboratory.
• To coordinate testing of the sample through Public Testing Laboratory (PTL).
• Maintain lab compliance w.r.t. Data Integrity, Computer System Validation (CSV), and GDP.
• Procurement of lab supplies, inventory, and services from approved vendors.
• Responsible to execute work done on Regional, Global, and Enterprise initiatives in
• Analytical Laboratory and ensure Standard and Global Procedures are implemented.
  Responsible to maintain the laboratory’s all-time Audit-Ready for Internal and External Audits.
• To ensure operation, upkeep, qualification, calibration & maintenance of analytical instruments like HPLC, FTIR, UV-Vis Spectrophotometer, etc.
• Ensure timely closure of Quality control-related investigations, CAPA, change controls OOS/OOT, and market complaints.
• To coordinate shift operation activities in QC Lab.
• Responsible for training of self and Lab Training Management and to initiate and complete qualification process of Analyst.
• To review Lab Testing data and provide disposition status of Raw Material and Packing Material on time.
• Responsible for review and Maintenance of Volumetric Solutions and Reagents/ indicators used during the analysis in the Laboratory.
  Ensure safe working practices are followed in lab as per EHS guidelines.
• Lab upkeep and 5S management in the lab.
• To conduct and ensure on time sampling & testing for incoming materials, in-process materials/products and finished products being manufactured in the plant.
• Review & revision of applicable SOPs, RM, FP and PM specifications.
• Responsible for RM, PM & FG reference sample management.
• Responsible for management of shade cards.
• To reviews laboratory cleaning records and destruction of post-analysis samples.
• Responsible for verification of periodic reviews of chemicals

Additional Responsibilities

• Actively participate in routine testing activities, as needed.
• Authors and revises procedures under minimal supervision. To take lead on document stream-lining.
• Follow all safety rules and regulations and conducts periodic safety audits.
• Follow all cGMP rules and regulations.
• Will perform work under minimum supervision and will provide oversite to projects and assist other chemists as needed.
• To interact with chemists and other personnel regarding testing, procedures performed, related results and prepare reports. Works to learn and improve on others’ techniques
• and tasks.
• To performs data generation, analysis, and problem solving with minimal rework.
• Reviews and assesses deviations; includes performing risk assessments, participating in root cause analysis investigations, tracking, follow-up, and reporting.
• Works under minimum supervision to ensure all work performed is executed in compliance with standard operating procedures, good manufacturing practices, and applicable regulations.

Apply Online

Editors Note: Johnson & Johnson Officer Quality Subscribe to Rasayanika for the latest chemistry and Pharma job openings, follow us on Facebook and Telegram and subscribe to our youtube channel for the latest updates on chemistry and Pharma jobs and much more.