Top 12 Control chemist Jobs in Cambridge, Ma

Scientist I, Quality Control
Replimune —Framingham, MA
- $112,500 - $146,000 a year
- Full-time
- Microsoft Word
- 5 years
- Computer literacy
- Paid holidays
- Health insurance
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8d
Scientist I, Analytical Development and Quality Control
Kailera Therapeutics, Inc. —Waltham, MA
- $106,000 - $130,000 a year
- Full-time
- Hybrid work
- Mid-level
- Master's degree
- 8 years
- Commuter assistance
- Paid holidays
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Research Associate II, Quality Control
Ocular Therapeutix —Bedford, MA
- $85,000 - $93,000 a year
- Research
- Mid-level
- Bachelor's degree
Quality Control Analyst I, Raw Materials
Ocular Therapeutix —Bedford, MA
- $68,000 - $75,000 a year
- Bachelor's degree
- Organizational skills
- Ability to lift 25 pounds
Sr. Research Associate, Preclinical Quality Control in Research Analytics
Moderna, Inc. —Cambridge, MA
- $74,000 - $118,400 a year
- Full-time
- Bachelor of Science
- Senior level
- 2 years
- Paid time off
- Adoption assistance
10d
Senior Scientist I, Quality Control
Candel Therapeutics —Needham, MA
- $155,000 - $160,000 a year
- Full-time
- Doctor of Philosophy
- US work authorization
- Computer skills
Research & Process Development Scientist
Parker Hannifin Corporation —Woburn, MA
- $100,300 - $166,900 a year
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
- Paid parental leave
- Paid holidays
Associate Director, Analytical Development and Quality Control
Kailera Therapeutics, Inc. —Waltham, MA
- $155,000 - $190,000 a year
- Full-time
- Hybrid work
- 5 years
- Bachelor's degree
- Travel
- Commuter assistance
- Paid holidays
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6d
Scientist II, Antisense/siRNA and Peptide Purification
Biogen —Cambridge, MA
- $117,000 - $157,000 a year
- Full-time
- Mid-level
- Master's degree
- Analysis skills
- Paid parental leave
- Employee stock purchase plan
Principal Scientist/Associate Director, Process Chemistry
Kymera Therapeutics —Watertown, MA
- $160,000 - $240,000 a year
- Bachelor of Science
- 11+ years
- Bachelor's degree
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Post-Doctoral Scientist – Mechanistic Modeling & Simulation(SMDD)
Eli Lilly —Boston, MA
- $58,000 - $123,200 a year
- Full-time
- Doctor of Philosophy
- US work authorization
- Senior level
- Health insurance
- Dental insurance
5d

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Scientist I, Analytical Development and Quality Control
Kailera Therapeutics, Inc. —Waltham, MA
Experience with data analysis tools (e.g., Excel advanced functions, JMP, or statistical software) for trending and visualization.
$106,000 - $130,000 a year
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Pr. Associate Scientist/Scientist I, Analytical Development
Solid Biosciences —Charlestown, MA
Bachelor’s degree in Molecular Biology, Biochemistry, Genetics or related field and 6-8+ years’ experience in analytical development within a biotech/…
$110,000 - $135,000 a year
Quick Apply

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Quality Control Chemist I
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Bachelor’s degree in chemistry or related field required. Coordinates with departmental leaders to develop appropriate corrective actions resulting from…

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Scientist I, Quality Control

Replimune -
Framingham, MA

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Job Details

Full-time
$112,500 - $146,000 a year
8 days ago

Benefits

Paid holidays
Health insurance
Dental insurance
Vision insurance
401(k) matching

Qualifications

Microsoft Word
Computer operation
Computer literacy
Bachelor's degree
GMP for research safety and compliance

Full Job Description

Overview

Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it.

At Replimune, we live by our values:

United: We Collaborate for a Common Goal.

Audacious: We Are Bold.

Dedicated: We Give Our Full Commitment.

Candid: We Are Honest With Each Other.

People are at the center of everything we do, and when it comes to our employees, we make it personal. With a deep sense of purpose, a strong and evolving culture, a competitive and forward-looking total rewards program, everyone at Replimune has a unique opportunity to impact on the lives of patients, caregivers and themselves.

Join us, as we reshape the future.

Job Summary:

The Scientist I/II, QC Analytical will perform QC testing according to Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP). This role may also include the responsibility of overseeing the work of junior QC staff and provide training for new analyst. The QC Analytical Scientist will be responsible for assisting with maintaining systems for QC Analytical Laboratory. The QC Analytical Scientist will be required to assist with scheduling, performing and reviewing of tests results of raw materials, in-process, drug substance and final drug product samples following established test method (SOPs). The QC Analytical Scientist will assist in the management of the QC laboratory. It is expected that the QC Scientist will maintain GMP compliance in the QC laboratory.

This position is based in our Framingham location and typically has a 5-day on-site expectation.

Responsibilities

Key responsibilities:

The responsibilities of the QC Analytical Scientist include, but are not limited, to the following:

Establish, revise and maintain procedures for QC Analytical testing.
Maintain QC systems related to raw materials, in-process, drug substance and final drug product sample testing.
Review testing data of other analysts.
Assist with the maintenance of QC laboratory and equipment.
Responsible for the protocol and report generation of method qualifications related to QC tests.
Perform QC Analytical testing of raw materials, in-process, water and product samples following Standard Operating Procedures (SOPs).
Review and complete documentation in accordance with current Good Manufacturing Practices (cGMP).
Responsible for change control, deviations and CAPA’s related to QC Analytical operations including conducting OOS, OOT, and lab investigations.
Assist with audits and regulatory inspections, as needed.
Assist with QC laboratory equipment validation.
Interact within internal, as well as across other functional groups to communicate QC Analytical requirements.
Oversee sampling and storage of QC samples and maintain regulatory/retention inventory.
Coordinate shipping of samples to contract testing laboratories.
Train of others within department within the scope of knowledge and responsibilities.
Understanding of USP/EP monograph testing/requirements.

Other responsibilities

Troubleshoot equipment and analytical test methods.
Manage technical studies performed with external companies with provision and review of reports.
Represent QC at inter-departmental meetings and interact with external vendors, as necessary.
Other tasks as assigned.

Qualifications

Education:

BA or BS in analytical chemistry or other related science, preferably with chemistry or coursework as part of the study program.

Required Experience:

5+ years of experience working in GMP/GLP environment or similar set up.
Knowledge of Analytical techniques and technical experience, within a Analytical Lab is preferred.
Computer literacy (MS Word and Excel), good communication and organizational skills.
Ability to work well independently and with others in a team.
Good organizational skills

Replimune is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is $112,500-$ $146,000. The exact base pay offered for this role will depend on various factors, including but not limited to the selected candidate’s unique set of qualifications, skills, and experience. Our current organizational needs also play a part in determining your final offer.

At Replimune, base pay is only one part of your total compensation package. The selected candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Replimune also offers various benefits offerings, including, but not limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays including year-end shutdown.

About Replimune

Replimune Group, Inc., headquartered in Woburn, MA, was founded in 2015 with the mission to transform cancer treatment by pioneering the development of a novel portfolio of oncolytic immunotherapies. Replimune’s proprietary RPx platform is based on a potent HSV-1 backbone intended to maximize immunogenic cell death and the induction of a systemic anti-tumor immune response. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response. The RPx product candidates are expected to be synergistic with most established and experimental cancer treatment modalities, leading to the versatility to be developed alone or combined with a variety of other treatment options. For more information, please visit www.replimune.com.

We are an Equal Opportunity Employer.

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Refine Your Search

control chemist jobs in cambridge, ma

Scientist I, Quality Control

Scientist I, Analytical Development and Quality Control

Research Associate II, Quality Control

Quality Control Analyst I, Raw Materials

Sr. Research Associate, Preclinical Quality Control in Research Analytics

Senior Scientist I, Quality Control

Research & Process Development Scientist

Associate Director, Analytical Development and Quality Control

Scientist II, Antisense/siRNA and Peptide Purification

Principal Scientist/Associate Director, Process Chemistry

Post-Doctoral Scientist – Mechanistic Modeling & Simulation(SMDD)

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