Jobs at Syner-G

You'll lead **technical operations** for the **Raleigh-Durham region**, driving **client satisfaction** and growth across a diverse portfolio of life sciences projects. Your core impact is developing the regional account strategy and building high-performing engineering teams. This role stands out with a supportive culture and recognition as a BioSpace Best Place to Work.

You'll join a **biopharma product development** team that accelerates **drug discovery and delivery**. Your work supports clients from critical R&D phases through commercialization. This role offers **meaningful impact** in a culture recognized as a "Best Place to Work."

You'll guide clients through **regulatory affairs** and **clinical development** activities, from early-stage to post-approval. Your impact includes leading FDA meetings and optimizing submission pathways. This role offers a chance to mentor new employees and shape strategy across diverse therapeutic areas.

You'll lead **design and optimization** of automated manufacturing systems for a **biopharma partner**. Your work will directly impact **life-enhancing therapy delivery** and ensure regulatory compliance.

You'll **lead validation system implementations** like **ValGenesis** in a **GxP pharmaceutical environment**, bridging business and technical stakeholders. Your work will accelerate life-enhancing therapies from discovery to delivery.

You'll own **end-to-end hourly payroll processing** and support exempt payroll as needed. You'll contribute to **ADP system projects** and help expand global payroll operations including India. This role offers **hybrid flexibility** with one in-office day per week.

You'll oversee maintenance and troubleshooting of facility systems in GMP laboratory and manufacturing environments. You'll coordinate service providers, perform inspections, and ensure compliance. This role offers **exposure to biopharma operations** and **collaboration with cross-functional teams** in a **life-enhancing workplace**.

You'll lead **facility operations** for a **biopharma product development partner**, overseeing complex systems and GMP compliance. Your work ensures safe, reliable operations across lab and manufacturing environments. This award-winning company offers a **life-enhancing career** with strong growth opportunities.

You'll lead **complex construction and engineering projects** from planning through commissioning for a **biopharma product development partner**. Your core impact is ensuring on-time, on-budget delivery with quality and regulatory compliance.

You'll generate and execute life cycle documentation for **qualification of equipment and processes** at Syner-G, a biopharma product development partner. Your core impact is driving **quality performance and compliance** across the organization. This role stands out with a **supportive culture and career growth** in a "Best Places to Work" award-winning environment.

You'll oversee **construction and engineering projects** for a **biopharma product development partner**, coordinating schedules, budgets, and safety from planning through closeout. Your core impact is ensuring **successful project execution** for life-enhancing therapies.

You'll coordinate construction and maintenance projects, **supporting safety teams** and ensuring compliance. Your work directly impacts **life-enhancing therapy delivery**. Join a **renowned biopharma partner** with a top workplace culture.

You'll design **stable formulations** for high-concentration subcutaneous dosage forms and optimize **lyophilization processes** for clients. Your work will directly support **regulatory submissions** and clinical development across all phases. This role offers collaboration with a top CMC team and recognition as a **Best Place to Work**.

You'll work on **accelerating breakthrough science** in oligonucleotide and peptide therapeutics, partnering with cross-functional CMC teams. Your role ensures analytical methods meet regulatory standards for **clinical development phases**. This position offers flexibility with remote work and a culture recognized as a "Best Place to Work."

You'll lead **commissioning, qualification, and validation** of GMP facility systems in a **biopharma environment**. Your work ensures safe, compliant, and inspection-ready operations for life-enhancing therapies.

You'll **perform equipment qualifications** including IQ, OQ, and PQ in a **GMP-regulated biopharma environment**. Your work will directly support **validation of automated production systems** for life-enhancing therapies.

You'll perform advanced maintenance on **GMP and non-GMP facility systems** and **utility equipment** like HVAC, boilers, and WFI systems. You'll troubleshoot complex issues independently and collaborate with cross-functional teams to support compliant operations.

You'll lead **capital projects** for facility expansions and infrastructure upgrades in a **biopharma product development and delivery** environment. You'll manage scope, schedule, and budget to ensure safe and efficient project execution. This role offers exposure to diverse client engagements and a culture recognized as a **"Best Places to Work"** award winner.

You'll manage building and plant operations, including labs and manufacturing utilities. You'll perform routine inspections, maintain documented records, and be on-call for emergencies. This role supports **GMP cleanroom environments** and ensures **compliance with regulatory requirements**.

You'll support **GMP facility systems** and **building utilities** for a life-sciences partner. Your work ensures **reliable operations** across lab and manufacturing environments.

You'll author **Clinical Study Reports**, study protocols, and submission materials for a **biopharma product development partner**. Your work directly supports client regulatory strategies, ensuring high-quality deliverables that accelerate drug approval. This role offers exposure to diverse document types and strong mentorship in a company recognized as a **"Best Places to Work"**.

You'll provide **executive-level leadership** and **strategic direction** for large capital programs in the biopharma sector. Your core impact involves establishing governance and driving **cross-functional alignment** to deliver projects safely and efficiently.

You'll lead **process optimization** for **oral solid dose manufacturing** at Syner-G, supporting tech transfer and commercial production. You'll **troubleshoot complex deviations** and drive continuous improvement across client programs.

You'll support **capital project buildout** of a new fill-finish suite within a commercial manufacturing facility. You'll partner with operations, QA, validation, and engineering to ensure robust, compliant manufacturing performance. This role offers the opportunity to work on **life-enhancing therapies** at a top biopharma partner.

You'll lead the **AI transformation strategy** at a biopharma product development partner. You'll define the AI vision and drive enterprise-wide adoption across business units. This role offers **high autonomy** and impact on **life-enhancing therapies**.

You'll lead the design and qualification of a **new commercial fill-finish suite** for a **top biopharma client**. Your work will directly **accelerate the delivery of life-enhancing therapies** to patients. This role offers a chance to partner across operations, QA, and validation in a GMP environment.

You'll lead and expand strategic regulatory partnerships at Syner-G, focusing on post-approval lifecycle management and driving integrated client solutions. You'll shape how regulatory services are delivered across the organization, positioning the company as a trusted partner to global pharma and biotech clients. This role connects **scientific expertise** with **strategic advisory** and **commercial growth**.

You'll lead **global regulatory strategies** for assigned products, ensuring **life-cycle management** and **submission execution**. You'll drive high-quality deliverables across US, EU, and other markets.

You'll guide clients through the development and execution of **Operational and Business Excellence programs**, driving sustainable transformation. Your core impact is translating strategy into actionable goals and coaching teams on **Lean Six Sigma methodologies**. You'll partner with leadership to shape long-term transformation roadmaps.

You'll lead **GCP quality and compliance engagements** for virtual and emerging biotechs, ensuring clinical programs are inspection-ready. You'll drive **sponsor oversight strategy** and serve as the embedded clinical quality voice across Phase 1-3 trials. This role offers **direct client-facing accountability** without people management.

You'll oversee clinical supply operations for a **biopharma product development partner**, supporting life-enhancing therapies from drug discovery to commercialization. Your leadership will directly impact project success and patient outcomes. This role offers **remote flexibility** and a **best-place-to-work culture**.