Duration & Type: 9 months Contract with a major pharmaceutical industry client
Location: San Diego, California
Responsibilities:
- Responsible for the development of new oligo or Reagent/Sub Assembly processes, transfer into Production and continuous improvement of existing processes.
- Provides oligo or Reagent/Sub Assembly process support to other Operations Groups.
- Provides support to Operations groups
- Assists in the development of manufacturing processes to transfer oligos or reagents/sub-assemblies to Manufacturing
- Assists with the creation of documents/change control packages in support of the transfer process.
- Coordinates these with the Technical Writer if applicable.
- Executes process validation protocols
- Originates simple change controls
- Participates in cost savings and process improvement activities
- Installs and validates new instruments or equipment.
- Participates in the notebook, development and pilot builds per written directions
- Completes ERP and cycle count transactions
- Stocks and maintains lab supplies
- Keep accurate records and documents
- Maintains lab under cGMP conditions
Required:
- Education: Bachelor’s Degree in BS degree, or equivalent, in chemistry, biology, biochemistry
- Knowledge of cGMP/GLP
- Proficiency with MS Word and Excel
- Intermediate Change Control skills
- Working knowledge of the appropriate analytical techniques (either for oligos or reagents)
- Strong math skills
For consideration, please send resume to career@infoquestgroup.com