×
Register Here to Apply for Jobs or Post Jobs. X

Analytical Scientist

Job in California, Moniteau County, Missouri, 65018, USA
Listing for: TryApplyNow
Full Time, Contract position
Listed on 2026-06-12
Job specializations:
  • Pharmaceutical
Salary/Wage Range or Industry Benchmark: 68000 - 85000 USD Yearly USD 68000.00 85000.00 YEAR
Job Description & How to Apply Below
Location: California

# Analytical Scientist Bora Pharmaceutical Services Full Timemid

CAPosted Yesterday##

Role Overview Bora Pharmaceutical Services is hiring a mid-level Analytical Scientist. This is a full-time role in CA. Part of Bora Pharmaceutical Services's Qa hiring, posted yesterday. Full responsibilities, required qualifications, and the apply link are listed in the description below.## Salary Context Salary is not disclosed in this posting. Market median for Mid-level Qa roles is $80k-$110k (based on 198 comparable listings).

Many employers share specifics during the interview process or after an initial screen.## Resume Keywords to Include Make sure these keywords appear in your resume to improve ATS scoring

OR Accessibility Compensation Benefits Bora Pharmaceuticals CDMONorth

Sign up free to auto-tailor your resume with all these keywords and get a higher ATS score##

Job Description About Bora Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in formulation development, clinical and commercial manufacturing, and packaging of complex oral solid dose, liquid, semi-solid, biologics, and sterile injectable pharmaceutical products. From our world-class sites in North America and Asia, we deliver drug products with unparalleled quality to more than 100 markets around the world.

Bora’s teams, technologies, and facilities work seamlessly together to enable our clients to deliver much-needed therapeutics to patients worldwide. At Bora Pharmaceuticals, we see it as our mission, our duty, our responsibility, to make our success and our customer’s success more certain.

Position Status This is an 18-month fixed-term contract (FTC) and a backfill position. The role is an active, approved vacancy within the organization and is intended to be filled as part of current staffing needs.

General Description Responsible for analytical method development and validation, analytical testing of drug substances and drug products, cleaning validation studies in support of the new development projects. Make detailed observations, review documents, and communicate test results.### Responsibilities
* Perform routine analytical testing, method transfer, method validation and test stability batches of drug products and drug substances.
* Responsible for timely execution of method development and validation to support Client’s needs.
* Author protocols and technical reports related to method development, method validation, method transfer and analytical cleaning validation.
* Ensure all analytical results and documentation are of high quality, generated in a timely fashion and comply with cGMP.
* Conduct analytical data and reports review in a timely manner.
* Provide technical expertise in support of OOS/OOT deviations.
* Actively participating and/or leading RCA to resolve/trouble shoot technical problems.
* Maintain extensive lateral contacts within and outside Bora.

Experience and Skills
* 3 years’ experience in the pharmaceutical industry.
* Capable of operating analytical lab equipment (i.e., HPLC, Dissolution, GC) relevant to job.
* Good understanding of analytical method development and validation.
* Excellent oral and written communication.
* Excellent computer skills.
* Proven ability to manage tasks and meet timelines.
* Good working knowledge of cGMPs, ICH and regulatory requirements for highly regulated markets.
* Is a team player and can work across all levels and functions.
* Well-developed multitasking abilities and strong collaborative skills.###

Education Required:

* Minimum Bachelor of Sciences in Chemistry or equivalent experience in the pharmaceutical industry.### Preferred
* MSc in Chemistry or equivalent with 3 years’ experience in the pharmaceutical industry.

Working Conditions
* On site role.
* Working in GMP lab environment.
* Use of appropriate PPE to prevent exposure to hazardous materials.
* Standrad 37.5 work week.

Additional Information In accordance with Ontario’s pay transparency requirements, candidates will be notified when they are no longer under consideration or once the vacancy is closed. Updates regarding application status may be communicated via email…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary