Associate Scientist (Entry level)

Aequor; West Greenwich (RI); On-site; USD 60,000 - 75,000; Full time

Job summary

Aequor is seeking an Associate Quality Control on-site in West Greenwich, RI for a 12-month contract. Responsibilities include performing routine QC procedures, sample collection, data entry, and equipment operation, with cGMP and CFR compliance.

Bachelor's degree required; lab experience preferred; benchtop testing with GC-MS and HPLC is a plus; shifts 7am–3:30pm or 8am–4:30pm, 100% onsite.

Qualifications

• Bachelor’s degree required.
• Some lab experience preferred.
• Benchtop testing with GC-MS/HPLC is a nice-to-have.

Responsibilities

• Perform routine laboratory procedures to support testing in Quality Control.
• Collect and handle samples, support testing equipment and laboratory operations.
• Maintain and operate specialized equipment; document, compute, and enter data into computerized systems.
• Initiate and/or implement changes in controlled documents; ensure safety guidelines and cGMPs/CFRs compliance.

Skills

Analytical skills

Attention to detail

Can-do attitude

Education

Bachelor’s degree

Tools

GC-MS

HPLC

Job description

Job Title: Associate Quality Control (Onsite Job in West Greenwich RI)

Duration: 12 Months with possible extension

Terms: Contract W2

Description:

100% onsite Rhode Island.

Shift (7am -3:30pm or 8am -4:30pm)Candidate can select their shift.

1 year duration with possible extension.

Ideal:

Bachelor’s degree required, internship experience preferred but Academic experience is also fine. Candidates must have some lab experience. Nice to have benchtop testing with instruments like GCMS HPLC.

Under general supervision, this position will perform routine procedures to support testing within Quality Control. Tasks may include but not limited to performing sample collection, sample handling, testing equipment/laboratory support. This position will be responsible for one or more of the following activities: - Performing routine laboratory procedures - Documenting, computing, compiling, interpreting, and entering data into computerized systems- Maintaining and operating specialized equipment - Initiating and /or implementing changes in controlled documents. Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory notebooks. Skills: some lab experience is preferred.

Top 3 Must Have Skill Sets:

• Strong Analytical Skills – Ideal candidate will have at least 4 years of experience performing analytical testing
• Attention to Detail – Ideal candidate will be thorough and deliver polished work product.
• Can Do Attitude – Ideal Candidate will have a positive attitude and be willing to participate in lean initiatives on site.