Contract Recruiter - Technical Operations & Engineering (Biotech/Pharma/Life Sciences)
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We are seeking an experienced Contract Recruiter to join our Talent Acquisition team for a 3-month engagement. This individual will focus primarily on pipelining and recruiting highly specialized Technical Operations and Engineering talent within the biotechnology, pharmaceutical, and life sciences industries.
The ideal candidate brings strong knowledge of the biotech talent market and has demonstrated success sourcing and recruiting technical professionals across areas such as Validation/CQV, Capital Projects, Facilities & Utilities, Engineering, Manufacturing, and related GMP-regulated functions.
This is a hands-on recruiting role requiring someone who can quickly understand technical requirements, proactively identify qualified talent, build strong candidate pipelines, and partner effectively with hiring managers and business leaders.
Key Responsibilities:
- Manage recruiting for Technical Operations and Engineering positions, from intake and sourcing through screening and interview coordination.
- Recruit for specialized roles including Validation Engineers, CQV Engineers, Capital Project Managers, Facilities Engineers, Reliability Engineers, Process Engineers, Project Engineers, and other technical positions supporting biotech and pharmaceutical operations.
- Develop targeted sourcing strategies to identify passive technical talent within the biotech, pharmaceutical, and life sciences markets.
- Proactively build pipelines for current and anticipated hiring needs, including roles requiring specialized GMP, manufacturing, engineering, and capital project experience.
- Conduct candidate screens to assess technical experience, project background, industry knowledge, availability, compensation expectations, and overall alignment with client and business needs.
- Partner closely with hiring managers and business leaders to understand technical requirements, project needs, timelines, and candidate profiles.
- Provide market insights regarding candidate availability, compensation, competitive hiring activity, and sourcing challenges.
- Maintain accurate and timely candidate and requisition information within the Applicant Tracking System (ATS).
- Deliver a high-quality candidate and hiring manager experience through consistent communication and effective management of the recruiting process.
- Balance multiple searches and shifting priorities in a fast-paced, project-driven environment.
Qualifications and Requirements:
Education:
- An Bachelor’s degree is preferred.
Technical Experience:
- 5+ years of recruiting experience, with significant experience recruiting technical or engineering professionals within the biotechnology, pharmaceutical, life sciences, or regulated manufacturing industries.
- Demonstrated experience recruiting roles such as Validation/CQV Engineers, Facilities Engineers, Reliability Engineers, Capital Project Managers, Process Engineers, Utilities Engineers, and/or other Technical Operations professionals.
Knowledge, Skills, and Abilities:
- Strong understanding of the talent landscape supporting GMP manufacturing environments, capital projects, facilities/utilities, commissioning, qualification, and validation.
- Proven ability to source specialized passive candidates using LinkedIn Recruiter and other sourcing tools and techniques.
- Experience managing multiple technical requisitions simultaneously while maintaining urgency and candidate quality.
- Strong ability to understand technical job requirements and translate them into effective sourcing strategies.
- Excellent communication, relationship-building, and candidate management skills.
- Ability to work independently and quickly become productive with limited ramp-up time.
- Experience with Greenhouse or a similar ATS preferred.
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Syner-G BioPharma Group
View Company ProfileSyner-G BioPharma Group (operating under synergbiopharma.com) is a leading global provider of integrated scientific, technical, regulatory, and compliance consulting services for the pharmaceutical, biotechnology, and medical device industries. Founded in 2007 by seasoned pharmaceutical scientist Dr. Prabu Nambiar, the company operates as a premier strategic development and delivery partner, guiding innovators through the complex multi-phase drug development lifecycle from pre-clinical Investigational New Drug (IND) milestones to post-approval commercialization. Syner-G's core architecture revolves around its proprietary CMC 360™ framework, an end-to-end technical offering covering Chemistry, Manufacturing, and Controls (CMC) technical operations, regulatory affairs strategy, medical writing, and rigorous cGxP quality compliance. The company operates a functional outsourcing and strategic advisory model, partnering closely with clients to apply Quality by Design (QbD) principles and build seamless operational bridges with Contract Development and Manufacturing Organizations (CDMOs) across small molecules, large molecule biologics, cell and gene therapies, and advanced virology programs. Backed by a growth equity investment from Boston-based private equity firm Riverside Partners, Syner-G has expanded its international delivery capacity significantly through targeted integrations, including the acquisitions of Sequoia Biotech Consulting and RMC Pharmaceutical Solutions. Further driving innovation, in mid-2026 the firm launched 3D Intelligence (3Di), a people-centered artificial intelligence transformation service tailored specifically to streamline biopharma documentation and development workflows. Consistently recognized by BioSpace as one of the industry's premier workplaces, the organization is headquartered in Framingham, Massachusetts, and leverages a global, distributed network of over 400 specialized bio-pharmaceutical consultants, engineers, and regulatory compliance strategists across North America, Europe, and the Asia-Pacific region.
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