Scientist (Devens) Job at Bristol Myers Squibb, Devens, MA

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  • Bristol Myers Squibb
  • Devens, MA

Job Description

Job Title: Scientist

Location: Devens, MA

Duration: 12 months

Pay range: $70 to $75.21/hr on W2

Onsite/hybrid: 50% onsite (Tue, Wed, Thurs). First month will need to be onsite every day.

Work hours: 40 hours, Core hours are 9:00 - 4:00

Top 3 to 5 Skills or Must haves:

  • Demonstrated Technical Writing Ability.
  • Worked in Cross matrix Teams.
  • Project Management - fast paced environment and can manage multiple projects at once.
  • Independent Contributor - personable and can work with multiple stakeholders.
  • Change Controls - GMP environments preferred.
  • Investigation Experience.
  • Bio Pharma experience preferred.

Job Description:

  • The Scientist in Manufacturing Sciences & Technology will support the Materials and Cryogenics Science group in the life cycle management of raw materials, consumables and single-use systems utilized for biopharmaceuticals commercial manufacturing operations. The successful candidate will collaborate closely with Manufacturing, Manufacturing Technology, Quality Assurance, Quality Control, Supply Chain, and Global Procurement groups on cross-functional teams.

The subject matter expert for this position will be primarily required to:

Qualify alternative raw material suppliers:

  • Work with procurement to identify new suppliers.
  • Recommend and/or lead necessary testing to qualify material for use in GMP manufacturing.
  • Author technical equivalency assessments, specification comparisons and material characterization reports.
  • Support risk assessments.
  • Author change controls.

Additional Tasks would include:

  • Support material and consumable manufacturing investigations.
  • Evaluate and manage material associated supplier changes notifications to maintain GMP compliance.
  • Support material specification development.

Requirements:

  • Minimum BS/MS with 2+ years of industry experience post-graduation or PhD in Material Science Engineering, Chemistry or equivalent scientific background.
  • Awareness of cGMP compliance and regulatory agency requirements.
  • Demonstrated problem solving ability (familiarity with root cause analysis techniques and CAPAs a plus).
  • Strong organizational, oral communication and technical writing skills.
  • Effective team player and strong individual contributor.
  • Familiarity with analytical techniques (FTIR, SEM-EDS, etc.).
  • Knowledge of data trending and tracking, including use of statistical analysis software a plus

Travel requirements: No

Physical requirements: No

Additional Job Requirements:

  • Lab w/o blood & animal

Job Tags

Part time,

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