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Temporary Biopharmaceutical Engineering Jobs (NOW HIRING)

TekWissen LLC

Construction Manager

Portsmouth, NH · On-site

$65 - $70/hr

Temporary Assignment Work Type: Onsite * Daily on-site Construction Management for multiple ... Min 5-7 years working in Pharmaceutical Engineering Projects and Construction Management.

K2 Staffing, LLC

Estimating Manager

Sacramento, CA

$135K - $190K/yr

... or biopharmaceutical environments * Strong understanding of piping systems and equipment ... Bachelor's degree in Construction Management, Mechanical Engineering, Civil Engineering, or a ...

K2 Staffing, LLC

Estimating Manager

Cypress, CA

$135K - $190K/yr

... or biopharmaceutical environments * Strong understanding of piping systems and equipment ... Bachelor's degree in Construction Management, Mechanical Engineering, Civil Engineering, or a ...

K2 Staffing, LLC

Estimating Manager

Livermore, CA

$135K - $190K/yr

... or biopharmaceutical environments * Strong understanding of piping systems and equipment ... Bachelor's degree in Construction Management, Mechanical Engineering, Civil Engineering, or a ...

Actalent

Assistant Project Manager

Brookfield, CT

Work closely with clients, architects, engineers, subcontractors, and internal stakeholders. * Lead ... Experience with high-tech, semiconductor, biopharmaceutical, or clean room construction.

K2 Staffing

Estimating Manager

Cypress, CA

... or biopharmaceutical environments * Strong understanding of piping systems and equipment ... Bachelors degree in Construction Management, Mechanical Engineering, Civil Engineering, or a ...

K2 Staffing

Estimating Manager

Livermore, CA

... or biopharmaceutical environments * Strong understanding of piping systems and equipment ... Bachelors degree in Construction Management, Mechanical Engineering, Civil Engineering, or a ...

K2 Staffing

Estimating Manager

Sacramento, CA

... or biopharmaceutical environments * Strong understanding of piping systems and equipment ... Bachelors degree in Construction Management, Mechanical Engineering, Civil Engineering, or a ...

Bilfinger

Scaffold Leadman

Pineville, LA · On-site

$19 - $24.25/hr

Bilfinger's comprehensive portfolio spans the entire value chain, from consulting & engineering to ... A scaffold builder is responsible for building up and breaking down temporary scaffold structures ...

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Temporary Biopharmaceutical Engineering information

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How much do temporary biopharmaceutical engineering jobs pay per year?

As of Aug 16, 2026, the average yearly pay for temporary biopharmaceutical engineering in the United States is $92,956.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,500.00 and $114,000.00 per year, depending on experience, location, and employer.

What is the difference between Temporary Biopharmaceutical Engineering vs Temporary Biopharmaceutical Manufacturing Technician?

AspectTemporary Biopharmaceutical EngineeringTemporary Biopharmaceutical Manufacturing Technician
Required CredentialsBachelor's in Engineering or Life Sciences, relevant certificationsHigh school diploma or associate degree, technical certifications
Work EnvironmentDesign labs, R&D facilities, process development areasManufacturing floors, production lines, quality control labs
Employer & Industry UsageBiotech companies, pharmaceutical firms, contract research organizationsManufacturing plants, biotech production facilities, contract manufacturing organizations

Temporary Biopharmaceutical Engineering roles focus on designing, developing, and optimizing biopharmaceutical processes, often involving R&D and technical analysis. In contrast, Temporary Biopharmaceutical Manufacturing Technicians work directly on production lines, ensuring manufacturing processes run smoothly. Both roles are essential in the biopharmaceutical industry but differ in responsibilities, work environment, and required credentials.

What jobs can you get with a temporary biopharmaceutical engineering degree?

A temporary biopharmaceutical engineering degree can qualify you for roles such as process technician, manufacturing associate, quality control analyst, or research assistant in biopharmaceutical companies. These positions often require knowledge of GMP regulations, laboratory skills, and familiarity with bioprocessing equipment.

Are temporary biopharmaceutical engineers in demand?

Temporary biopharmaceutical engineers are in demand due to ongoing growth in the biotech and pharmaceutical industries, especially for roles involving process development, manufacturing, and quality assurance. Employers seek candidates with skills in bioprocessing, regulatory compliance, and familiarity with industry tools, making these positions relatively accessible for qualified professionals.
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What are the most commonly searched types of Biopharmaceutical Engineering jobs?

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What states have the most Temporary Biopharmaceutical Engineering jobs?

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Temporary Biopharmaceutical Engineering jobs near you
Infographic showing various Temporary Biopharmaceutical Engineering job openings in the United States as of August 2026, with employment types broken down into 91% Full Time, 4% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $92,956 per year, or $44.7 per hour.

Project Manager, Change Control (Contract) 665

Vertex Pharmaceuticals Incorporated

Boston, MA • On-site

$58 - $65/hr

Full-time

Posted 5 days ago

Vertex Pharmaceuticals rating

6.5

Company rating: 6.5 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

78th of 86 rated pharmaceutical

Job description


The Change Control Project Manager is responsible for supporting the cross-functional project teams executing change controls. The Project Manager will track and report project scope/timeline/milestone status associated with cell and gene therapy T1D team.
Must be detail-driven and have a proven history in managing and driving project success within the biotech industry. The individual requires a strong technical background, solid working knowledge of GMPs, understanding of the drug development pathway through commercialization, and willingness to pivot as priorities change. Knowledge and/or experience with cell / gene therapy methodologies and a strong understanding of risk management will be an asset. Must have excellent communication skills, written and verbal, high attention to detail, and the ability to work effectively in cross-functional, matrixed teams.
RESPONSIBILITIES
  • Partner closely with functional area leads, maintain and actively monitor integrated project plans. Identify/communicate interdependencies as well as critical path activities for the project(s)
  • Track and monitor key milestones and decision points and work with project team members to drive the completion of changes.
  • Effectively communicate with internal team members and key stakeholders on the status, objectives, risks, and mitigation plans associated with change control projects.
  • Write Risk Assessments
  • Organize and maintain team communications including meeting agendas, minutes, tasks lists, and risk analyses/mitigation strategies.
  • Update and maintain project status tools, such as a project action log and risk register.
  • Develop and deliver project management tools and templates to manage change control team activities.
  • Consistently perform duties within established SOPs, and in accordance with GxP requirements, where applicable

QUALIFICATIONS
  • Bachelor's degree in engineering, life sciences or related field.
  • A minimum of 8 years of experience in the biopharmaceutical industry.
  • A minimum of 6 years of experience in project management of biopharmaceutical product
  • Working knowledge of biotechnology, GMPs, and drug development lifecycle.
  • Ability to work effectively in cross-functional, matrixed environment, prioritizing and managing multiple tasks simultaneously, integrating cross-functional issues and balancing competing priorities effectively.
  • Expertise in Microsoft suite (Project, PowerPoint, SharePoint, Word, Excel, Outlook). Experience with other PM tools a plus (e.g., Smartsheet, Power BI, etc.).
  • Excellent oral and written communication skills, including presentation and facilitation skills, to effectively inform key updates & issues across all levels of the organization.
  • Strong analytical, problem solving and critical thinking skills, including an ability to combine attention to detail with a big picture perspective.
  • Strong understanding of regulatory requirements (FDA, 21 CFR Part 211, EU GMP, ICH Q10)

Pay Range
$58-$65/hr
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 privacyadministrator@atriumstaff.com.
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 tempstaffing@vrtx.com. Please include the job title in the subject of your email.
No C2C or Third-Party Vendors

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