Associate Chemist

Industry

Pharmaceuticals

Advert ID

FOX_BBBH31718

Location

Somerset

Job Type

Contract

Hours

Full-Time

Salary Range

Up to USD0.00 per year

No. of Openings

1

Branch Information

Raleigh Engineering - (USA) 701 Corporate Center Drive Suite 375 NC Raleigh , NC 27607

ContactNumber

919-755-5804

Job Description

Job Summary:





Performs routine analytical testing of pharmaceutical raw materials and finished products. Assist in developing and validating analytical methods for active pharmaceutical drug substance and drug products. Write and update SOPs, validation protocols, reports, test procedures and specifications. Maintain laboratory notebooks and lab instruments in compliance with internal SOPs and current USP, FDA guidance. Communicate results in written and oral presentations.



Job Responsibilities:





* Ability to validate analytical methods for drug substance and drug products as per approved protocols under supervision.

* Independently execute analytical test procedures for the analysis of raw materials and finished products.

* Write and review analytical method validation protocols, reports and technical documents.

* Write and update Analytical R&D SOPs

* Capable of self-scheduling of work assignments.

* Assures right-first-time execution of methods and SOPs.

* Provide support for ordering and maintaining inventory of laboratory material and equipment.

* Participate in inter-department task teams.

* Perform all other duties as assigned, or as business needs require.

Qualification and Requirements:



* BS or MS degree in chemistry, biology or other related scientific discipline required.

* 3+ years of experience in the pharmaceutical industry and has extensive knowledge of chromatographic techniques.

* Experience with pharmaceutical laboratory equipment such as HPLC, UV, GC, Dissolution, IR, etc. is required.

* Experience in executing USP and EP test methodology is required.

* Ability to work effectively under pressure to meet deadlines.

* Proficiency in word, excel, and pdf documents is a plus.

* Excellent attention to details

* Excellent verbal and written communication skills

* Good knowledge of FDA guidelines, ICH and related guidelines

* Ability to manage timelines and priorities

* Ability to establish and maintain good working relationships