EngineerScientist II, QC

Work Schedule

Environmental Conditions

Job Description

As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.

DESCRIPTION:
Join our Quality Control team at Thermo Fisher Scientific where youll make meaningful contributions to our mission of enabling customers to make the world healthier cleaner and safer. As an Engineer/Scientist II QC youll perform testing and analysis to ensure product quality while working with state-of-the-art analytical equipment in a GMP environment. Youll conduct testing of raw materials in-process samples and finished products using various analytical techniques evaluate test data document results and participate in continuous improvement initiatives. This role offers excellent opportunities for professional growth while working alongside colleagues who share your commitment to science and quality.

Location: West Hills CA. Relocation assistance is NOT provided.

• Must be legally authorized to work in the United Stateswithoutsponsorship.

• Must be able to pass a comprehensive background check whichincludes a drug screening

REQUIREMENTS:
Bachelors Degree plus 2 years of experience required preferably in pharmaceutical/biotech industry
Preferred Fields of Study: Chemistry Biochemistry Biology Molecular Biology or related scientific field
Additional certifications in Quality Control/GMP practices beneficial
Strong knowledge of GMP regulations and quality systems requirements
Proficiency in analytical techniques including HPLC GC MS spectrophotometry
Experience with microbiological and biochemical testing methods
Demonstrated expertise in data analysis and investigation of out-of-specification results
Strong documentation skills and proficiency with laboratory information management systems
Knowledge of relevant regulatory standards (ISO FDA USP EP)
Excellent attention to detail and ability to follow written/verbal procedures accurately
Strong organizational and time management skills
Ability to work both independently and collaboratively in a team environment
Proficiency in Microsoft Office applications
Clear written and verbal communication skills in English
Experience with laboratory automation systems preferred
Knowledge of Lean/Six Sigma principles beneficial

Compensation and Benefits

This position may also be eligible to receive a variable annual bonus based on company team and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on which includes:

• A choice of national medical and dental plans and a national vision plan including health incentive programs

• Employee assistance and family support programs including commuter benefits and tuition reimbursement

• At least 120 hours paid time off (PTO) 10 paid holidays annually paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave) accident and life insurance and short- and long-term disability in accordance with company policy

• Retirement and savings programs such as our competitive 401(k) U.S. retirement savings plan

• Employees Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits please visit: Experience:

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