Top 207 Associate Biotech/Chemical Jobs

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QC Raw Material Scientific Sr. Associate/Associate (Contract) 29416

Vertex Pharmaceuticals -
Boston, MA

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Job Details

Full-time
$35 - $48 an hour

Qualifications

Pharmaceutical company experience

Full Job Description

Job Description:

The QC raw material scientific/sr. scientific associate operates independently to perform raw material testing such as appearance and ID of materials including but not limited to small molecules, chemicals, solvents and gases. The associate will be responsible for supporting shipment of samples to external contract testing labs which includes - process and receipt in LIMS, packaging of samples at appropriate storage conditions, completion of respective vendor sample submission form, and processing of final results in LIMS/associated internal forms. The associate will also be responsible for performing particle characterization of foreign particulates found in various sample types (i.e. finished product, cryopreserved intermediate, water flushing). The ideal candidate will have expertise in particle analysis techniques and instrumentation as well as conducting various raw material analytical testing.

** The identified candidate will need to pass a vision and color blindness test **

Key Duties and Responsibilities:

Works with multiple functional groups to meet business needs.
Performs internal raw material testing per associated material specification to support GMP operations
Supports shipment of samples to external contract testing labs for respective testing per associated material specification
Characterize sub-visible and visible particulates by FTIR and optical microscopy
Individual should be capable of writing reports related to work completed in laboratory.
Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines.
Problem solving, either independently or with assistance pertaining to extraction of particulates and/or instrumentation problems.
Performs work assignments accurately, and in a timely and safe manner
Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP)
Performs self and peer review of the data for accuracy and compliance

Knowledge and Skills:

Team focused, demonstrate high level of integrity, and have strong collaboration, communication, interpersonal and organizational skills
Prior experience using FTIR and raw material testing experience
Knowledge of multiple applicable techniques such as: particle size, microscopy
Proficient in Microsoft Excel and Word
Proven ability in technical writing skills
Proven problem solving and troubleshooting abilities
Good written and oral communication skills
Ability to work in a collaborative work environment with a team
Experience being involved with analytical investigations/deviations

Education and Experience:

Bachelor’s degree in a biologic field, life sciences, engineering, chemistry, pharmaceutical science.
At least 5 years’ experience in the pharmaceutical industry, biotech industry, life sciences industry.
Particle ID and raw material experience is a plus

Work Hours

Standard Hours: Monday – Friday 8:00am - 4:30pm (with flexibility to support second shift / weekends as needed)

Pay Range:

$35-42/hr (Associate) $42-48/hr (Sr. Associate)

Requisition Disclaimer:

This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (“Vertex”). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements

By applying for this position, you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials, which may include your CV/Resume, email address or phone number, with Vertex. For more information on how Vertex handles your personal data related to your job application, please see Vertex’s Careers Privacy Notice. Agreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners

(collectively, “Atrium Alerts”). Atrium Alerts may be sent by email, phone, or text message. Your personal information will be safely stored within the Atrium & Vertex databases. Atrium does not sell your personal information to third parties. Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time, please contact Atrium at [email protected].

If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at [email protected]. Please include the job title in the subject of your email.

No C2C or Third-Party Vendors

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