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Avecia Jobs (NOW HIRING)

Nitto Denko Corp.

$107K - $130K/yr

Understand Nitto Avecia financial goals and pricing models to prepare client proposal pricing * Maintain constant territory demand and sales data in CRM and other designated databases * Utilize ...

Nitto Denko Corp.

$80K - $95K/yr

Support Customer QA SME along with department management in support of Avecia's Audit hosts during Regulatory or Client audits. * Support the review and negotiation of client specific quality ...

Nitto Denko Corp.

$95K - $116K/yr

Provide leadership to any direct reports that manage client manufacturing programs at Avecia. * Act as QA project representative along with department management on Client Manufacturing campaigns and ...

Nitto Denko Corp.

$135K - $165K/yr

Communicates with Avecia Executive oversights, cross-functional department heads, clients, and internal oligo process subject matter experts for peer review. * Plans and manages the use of T&I ...

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Avecia information

See salary details

$25K

$80.3K

$163.5K

How much do avecia jobs pay per year?

As of Jun 12, 2026, the average yearly pay for avecia in the United States is $80,287.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,500.00 and $103,000.00 per year, depending on experience, location, and employer.

What is Avecia and what does the company do?

Avecia is a biotechnology company that specializes in the development and manufacture of oligonucleotides, which are short strands of DNA or RNA used in research, diagnostics, and therapeutics. The company provides custom synthesis and large-scale manufacturing services for pharmaceutical and biotech companies developing nucleic acid-based drugs. Avecia is known for its expertise in process development, regulatory compliance, and delivering high-quality oligonucleotide products to support clinical and commercial needs.

What is the difference between Avecia vs Chemist?

AspectAveciaChemist
Required CredentialsBachelor's or higher in Chemistry, Chemical Engineering, or related fieldBachelor's or higher in Chemistry or related discipline
Work EnvironmentPharmaceutical and chemical manufacturing facilitiesLaboratories, research centers, manufacturing plants
Employer & Industry UsagePharmaceutical, biotech, and chemical companiesResearch labs, industrial manufacturing, academia
Common Search & ComparisonYesYes

Both Avecia and Chemist roles typically require a background in chemistry or related fields. While Avecia often refers to a specific company specializing in biopharmaceutical manufacturing, the term Chemist is more general and applies across various industries. The main differences lie in the context: Avecia is a company name, whereas Chemist describes a professional role. Understanding these distinctions helps job seekers target the right opportunities and clarify their career paths.

What types of projects and clients do team members at Avecia typically work with?

At Avecia, team members often work on projects involving the development and manufacturing of oligonucleotide-based therapeutics for pharmaceutical and biotechnology clients. The work environment is highly collaborative, with cross-functional teams handling research, process development, quality assurance, and large-scale production. Team members regularly interact with clients to provide updates, address technical challenges, and ensure project milestones are met. This exposure to a variety of projects and clients allows employees to broaden their technical expertise and gain valuable industry experience.

What are the key skills and qualifications needed to thrive as a Chemist at Avecia, and why are they important?

To thrive as a Chemist at Avecia, you need a solid background in chemistry or chemical engineering, typically supported by a relevant degree and laboratory experience. Familiarity with analytical instruments such as HPLC and GC, as well as knowledge of GMP (Good Manufacturing Practice) standards, is commonly required. Attention to detail, strong problem-solving abilities, and effective teamwork are important soft skills for success in this role. These competencies ensure accurate chemical analysis, safe and compliant operations, and efficient collaboration in a specialized chemical manufacturing environment.
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Avecia jobs near you
Infographic showing various Avecia job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% Physical job distribution, with an average salary of $80,287 per year, or $38.6 per hour.
Senior Quality Assurance Specialist, PPQ/Commercial QA Projects

Senior Quality Assurance Specialist, PPQ/Commercial QA Projects

Nitto Denko Corp.

Milford, MA

$95K - $116K/yr

Full-time

Posted 19 days ago

Job description

About this opportunity :
The Senior QA Specialist is responsible for interfacing with and provide quality input to client's manufacturing programs that are in late stages of development and/or commercialized. This includes interfacing with clients that are nearing process performance qualification (PPQ), PAI and commercial readiness, and that are approved to manufacture in global regions.
Key Responsibilities:
  • Provide leadership to any direct reports that manage client manufacturing programs at Avecia.
  • Act as QA project representative along with department management on Client Manufacturing campaigns and at client meetings (e.g., onsite and teleconferences) as directed by QA Project Team management.
  • Prepare responses to customer supplied QA agenda topics and lead discussions during client meetings ensuring that any outstanding questions relative to the agenda topics are discussed with QA department management.
  • Provide strong link/communication between the QA function/activities with all other departments at the Milford site.
  • Support the Customer QA SME along with department management in support of Avecia's Audit hosts during Regulatory or Client audits.
  • Support the review and negotiation of client specific quality agreements with sponsor and liaise with QA Regulatory Compliance to ensure that Avecia is in compliance with stated GMP regulatory commitments.
  • Ensure client specific Corrective and Preventative Actions are implemented in a timely fashion and provide updates to clients, as needed.
  • Responsible for reviewing quality records and Quality Assurance procedures.
  • Support the review and approval of client specific deviations and gathering/issuing quality metric reports to executive management.
  • Support customer complaint investigations, as needed, and follow up with customers on all technical complaints until closure/resolution is reached.
  • Perform disposition of advanced oligonucleotide products for pharmaceutical use, including pharmaceutical intermediates, active pharmaceutical ingredients (API) and adjuvants/constituent materials in accordance with approved specifications and procedures, including Avecia Enterprise Resource Planning System (SAP) transactions

Required Skills/Abilities:
  • BS/BA in science or equivalent work experience with 5+ years' experience in either GMP Production or Quality Assurance.
  • Ability to provide expert advice and sound decision-making on all aspects of cGMP. He/she must have a strong knowledge of the cGMP regulation and technical knowledge of the subject and the potential issues involved. This is achieved through a combination of experience in Quality Systems coupled with education and training in Quality Systems, cGMP, Quality audits, documentation, change control, corrective preventative action, validation, calibration, review of quality records, quality metrics, failure investigations and manufacturing and laboratory controls as per cGMPs.
  • As the regulatory and cGMP requirements frequently change, the jobholder must also maintain current knowledge.

The annualized salary range for this role is $95,300.00 - $116,600.00.

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