Our client, a world-leading Pharmaceutical Company in West Greenwich, RI is currently looking for a Sr. QC Associate (HPLC, Gas Chromatography) to join their expanding team.

Position Details:

• Job Title: Sr. QC Associate (HPLC, Gas Chromatography) / Pharma Industry
• Duration: 12 months contract, extendable up to 36 months
• Location: West Greenwich, RI

Note:

• The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
• You may participate in the company group medical insurance plan

Job Description:

• Candidate will be working on site
• Targeting candidates with 4-6 years of industry/ non academia experience and complex Instrumentation experience, including HPLC and GC
• Quality Control Raw Materials lab is searching is for an team member to support testing for raw material testing.
• This person will be responsible for working in the Quality Control laboratory, using GMPs and GDPs to execute analytical testing.
• The ideal candidate enjoys tackling challenges and excels at time management with attention to detail.

Job Requirements:
Responsibilities will include, but are not limited to:

• Performing analytical testing for HPLC, GC and ICP-MS
• Interacting cross-functionally with a wide variety of people and teams;
• Troubleshoot, solve problems and communicate with stakeholders.
• Participate in initiatives and projects that may be departmental or organizational in scope.
• Evaluate lab practices for compliance and operational excellence on a continuous basis.

Qualifications:

• 4-6 years of experience with lab instrumentation and/or Empower software
• Bachelors Degree in any science field
• Demonstrated experience in investigations and QC processes
• Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal supervision
• Strong communication skills (both written and oral), facilitation and presentation skills
• Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories, preferably with GMP experience
• Understanding of biopharmaceuticals process and related unit operations
• Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy
• Independent, self-motivated, organized, able to multi-task in time-sensitive environments.

Top 3 Must Have Skill Sets:

• GMP/QC experience (non-academia)
• HPLC, GC and/or ICPMS and chromatography data software
• Quality mindset in team environment

Day to Day Responsibilities:

• Routine testing and lab operations
• Maintaining training
• Problem solving

Employee Value Proposition:

• Great biotech/pharma to work for

Red Flags:

• Only academia experience with complex instrumentation
• Job variability

"Client requires all staff, staff augmentation external workers, and certain other external workers, in the United States and Puerto Rico to be vaccinated from COVID 19 as a condition of assignment. In accordance with applicable law, Client will provide reasonable accommodations to staff augmentation external workers who qualify on the basis of a medical reason or a sincerely held religious belief, practice, or observance. Such accommodation may not pose an undue hardship to client, its operations, or its staff.