Associate Scientist (Entry level)

Aequor; West Greenwich (RI); In loco; USD 54.000 - 72.000; Tempo pieno

Descrizione del lavoro

Aequor in West Greenwich, Rhode Island is hiring an Associate Quality Control professional for an onsite, 12-month contract (W2). The role requires a Bachelor's degree and some lab experience; benchtop testing with GCMS and HPLC is a plus.

Candidates may select day shifts (7:00–3:30) or (8:00–4:30). Under supervision, you will perform routine QC procedures, collect samples, document results, maintain equipment, and help update controlled documents.

Competenze

• Bachelor’s degree required; internship or academic lab experience acceptable.
• Some lab experience required; on-site testing experience preferred.
• Must learn and follow safety and cGMP/CFR guidelines.

Mansioni

• Perform routine laboratory procedures in Quality Control.
• Document, compute, and enter data into computerized systems.
• Maintain and operate laboratory equipment.
• Initiate and/or implement changes in controlled documents.

Conoscenze

Strong Analytical Skills

Attention to Detail

Can Do Attitude

Formazione

Bachelor’s degree

Strumenti

GCMS

HPLC

Descrizione del lavoro

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.