Chemist I

Job Description

Job Description

Actalent is hiring for a Chemist in the Scarborough, ME area!!

Job Description

This Chemist I position is a Technical Manufacturing Chemist role within an infectious disease developed markets business unit based in Scarborough, Maine. You will produce materials used in immunology-based chromatography and enzyme tests, support a regulated manufacturing environment, and contribute to product and process improvements while following established protocols and quality standards.

Responsibilities

• Maintain and support the production schedule to ensure timely manufacturing of bioreagents and materials used in immunology-based chromatography and enzyme tests.
• Investigate problem areas in the manufacturing process and identify opportunities for desirable improvements in methods, yields, and product performance.
• Undertake new procedures and follow proper safety precautions at all times in accordance with laboratory and facility safety guidelines.
• Perform in-process quality control (QC) testing of manufacturing materials, including qualification testing, quality inspections, and titration, to ensure products meet defined specifications.
• Maintain quality systems and adhere to Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) standards throughout all work activities.
• Create, interpret, and follow protocols focused on product improvement and process optimization.
• Prepare critical and non-critical bioreagents for use in products and manufacturing processes using established Standard Operating Procedures (SOPs).
• Work in a team setting to coordinate manufacturing efforts based on the production schedule, ensuring the raw bioreagent supply is maintained to meet ongoing manufacturing needs.
• Use laboratory equipment such as pipettes, spectrophotometers, HPLC systems, pH meters, and electrophoresis equipment as part of routine manufacturing and testing activities.
• Document work accurately and completely in appropriate records, forms, and electronic systems to support traceability and compliance.
• Collaborate with colleagues in manufacturing, quality, and other functions to resolve issues and support continuous improvement initiatives.

Essential Skills

• Bachelors degree in Chemistry, Life Sciences, or a related field, or an equivalent combination of education and experience.
• Hands-on experience using pipettes in a laboratory or manufacturing environment.
• Experience performing spectrophotometry for analytical or quality control purposes.
• Experience operating high-performance liquid chromatography (HPLC) systems.
• Experience using pH meters for solution preparation and testing.
• Experience with gel electrophoresis techniques, including SDS-PAGE.
• Experience performing ELISA assays.
• Ability to work successfully as a member of a team and independently with moderate supervision.
• Skill in using computer applications, including spreadsheet, database, manufacturing, and word processing software.
• Ability to follow Standard Operating Procedures (SOPs), GMP, and GLP requirements accurately and consistently.

Additional Skills & Qualifications

• Experience in immunology, biochemistry, or related life science disciplines is beneficial.
• Experience in a regulated manufacturing or laboratory environment is advantageous.
• Strong attention to detail and commitment to maintaining high quality standards.
• Ability to troubleshoot basic issues with laboratory equipment and processes.
• Effective communication skills for collaborating with cross-functional teams.
• Organizational skills to manage multiple tasks while supporting a production schedule.

Work Environment

This role is based in a laboratory and manufacturing environment in Scarborough, Maine, focused on infectious disease products and immunology-based chromatography and enzyme tests. You will work with a variety of laboratory instruments, including pipettes, spectrophotometers, HPLC systems, pH meters, and electrophoresis equipment such as SDS-PAGE setups, as well as ELISA assay platforms. The position involves following Standard Operating Procedures, GMP, and GLP requirements, and working within established quality systems. Work is performed in a team-oriented setting with moderate supervision, and you will use computer applications for data entry, documentation, and manufacturing-related tasks. The environment emphasizes safety, adherence to protocols, and collaboration to meet production schedules and maintain a reliable supply of bioreagents.

This is a Contract position based out of Scarborough, ME.

The pay range for this position is $28.00 - $30.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave)

This is a Contract position based out of Scarborough, ME.

This position is anticipated to close on Oct 28, 2026.

This is a fully onsite position in Scarborough,ME.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email View email address on ziprecruiter.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.