Who We Are
Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with.
How You'll Spend Your Day
- 24 7 audit readiness.
- Participation in internal, external, regulatory audits.
- Ensure 100% participation in training's against CAPA's.
- Responsible for initiation and investigation on LIR, OOS, OOT & boarder line results and reporting them to the in-charge.
- Supporting to share required documents from QC to RA/ other requirement.
- Determining team priorities in accordance with the plant's needs, while coordinating with the team leader /Manger.
- Follow up the housekeeping, cGMP, GLP and Safety Guideline in laboratory.
- Sampling and analysis of RM / FG / intermediates / cleaning samples based on requirement and result entry in analytical sheet, QA form, LIMS and online documentation as per data integrity norms.
- Perform analytical test according to the monograph and SOP.
- Responsible for calibration and verification of instruments.
- Maintaining of reserved samples room and chambers / autoclaves / incubators.
- Help to in charge in preparation of documents related to department (like STP's, SOP's and etc.)
- Ensure the sampling of finished products, Raw material, Intermediate and sending sample to outside laboratory for analysis.
- Must be ensured sampled, approved and rejected labels timely as required.
- Responsible to maintain the stock record of chemicals and reconciliation of standards.
- Any other job assigned by the Manger -QC Manger or group leader-QC
Your Experience And Qualifications
- Required B.Sc./ M.Sc. qualified candidate
- 3-6 years of relevant experience in HPLC with empower software
- Good understanding of Quality control, Understanding of GMP & GLP
- candidate will be flexible in shifts (24*7)
Reports To
Group Leader / Manager Quality
Teva's Equal Employment Opportunity Commitment
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.
