Attiva gli avvisi di lavoro via e-mail!

Sr. Specialist, Quality Assurance Operations

Moderna Therapeutics

Sacile

In loco

EUR 40.000 - 60.000

Tempo pieno

7 giorni fa
Candidati tra i primi

Descrizione del lavoro

A leading biotech company in Sacile is seeking a Sr Specialist QA Operations to ensure compliance in contract manufacturing and testing facilities. The successful candidate will provide quality oversight, approve documentation, and support quality investigations. The role requires a Bachelor's degree and 2-5 years of relevant experience. Knowledge of EU regulations and fluency in English and Italian are essential. Competitive benefits and well-being resources are offered.

Servizi

Quality healthcare and insurance benefits
Lifestyle Spending Accounts
Free access to fitness, nutrition, and mindfulness classes
Family planning and adoption benefits
Generous paid time off

Competenze

  • 2-5 years of quality industry experience required.
  • Experience in validation and CSV is advantageous.
  • Experience working with CMOs and relationship management preferred.

Mansioni

  • Provide QA oversight at contract manufacturing sites.
  • Review and approve cGMP documentation.
  • Support quality investigations and manage CAPA.

Conoscenze

Fluency in English
Fluency in Italian
Interpersonal skills
Analytical skills
Problem-solving

Formazione

Bachelor's degree in Sciences, Pharmacy, or Engineering

Strumenti

Knowledge of EU and global regulations
Experience in sterile manufacturing

Descrizione del lavoro

Reporting to the Senior Manager Quality Assurance (QA) Operations - Drug Product Team Lead for the International Organization, the Sr Specialist QA Operations will be responsible for providing QA oversight and support for contract manufacturing and testing facilities as well as internal functions to ensure compliance with internal policies and procedures and specifications, regulatory requirements.

The Sr Specialist QA Operations will support manufacturing and release at CMO’s site and ensure local cGMP and Moderna policies are effectively applied. The incumbent will provide person in plant QA presence at contract manufacturing organization (CMO) sites for oversight of drug product fill finish activities and support review and approval of all cGMP documentation including policies / SOPs, testing data, deviations, CAPA and Changes Controls The incumbent will participate to the transfer of product to the CMO’s site under the supervision of the Sr Manager or Manager QA.

  • Here’s What You’ll Do

Provide person in plant QA presence at contract manufacturing organization (CMO)

Review and approve cGMP documentation (SOPs, protocols, technical reports, specifications, deviations, CAPA, change controls).

Support quality investigations and manage CAPA (corrective and preventative actions) for CMO activities.

Review and coordinate approval of all changes made to the manufacturing, testing and control processes including those that are initiated by CMOs

Review batch records, and other documentation to ensure that all steps have been executed correctly, verified where applicable, and that all limits and specifications have been met and were conducted in accordance with regulatory filings, regulatory requirements and internal policies and procedures.

Collaborate with the Manager Operations QA to review and approve method, equipment and process validation protocols and reports to ensure compliance with approved acceptance criteria.

Provide QA oversight at contract manufacturing sites to ensure compliance with approved quality agreements and overall cGMP compliance for Moderna’s drug products.

This role might require ad-hoc international travel.

  • Here’s What You’ll Bring to the Table

Bachelor degree, preferably in Sciences or Pharmacy or Engineering with applied Quality industry experience of 2-5 years.

Working knowledge of relevant EU and global regulations.

Experience in sterile manufacturing, packaging and testing Experience in CSV and validation is an advantageous.

Fluency (written / spoken) in English and Italian - fluency in other languages is advantageous

Excellent interpersonal skills using a team-oriented approach to project management and problem solving for complex issue resolution in a scientifically sound and understandable way.

Outstanding communication skills (verbal and written) to all employee levels, executive leadership and external partners, suppliers, third parties, and industry organizations.

Experience working with CMOs, CLOs, vendors, and relationship management preferred

Ability to conceptualize, analyze, plan and manage multiple projects in a fast-paced environment.

Ability to be agile and effectively collaborate in a dynamic, cross-functional matrix environment.

Ability to navigate through ambiguity and rapid growth and adapt to change.

A ‘digital first’ and curious mindset that allows you to constantly learn and challenge the status quo.

Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.

We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with :

Quality healthcare and insurance benefits

Lifestyle Spending Accounts to create your own pathway to well-being

Free premium access to fitness, nutrition, and mindfulness classes

Family planning and adoption benefits

Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, and a discretionary year-end shutdown

Educational resources

Savings and investments

Location-specific perks and extras!

The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.

About Moderna

In over 10 years since its inception, Moderna has transformed from a research-stage company advancing programs in the field of messenger RNA (mRNA), to an enterprise with a diverse clinical portfolio of vaccines and therapeutics across seven modalities, a broad intellectual property portfolio in areas including mRNA and lipid nanoparticle formulation, and an integrated manufacturing plant that allows for rapid clinical and commercial production at scale. Moderna maintains alliances with a broad range of domestic and overseas government and commercial collaborators, which has allowed for the pursuit of both groundbreaking science and rapid scaling of manufacturing. Most recently, Moderna's capabilities hav

Quality Assurance Specialist • Sacile, Italia

Ottieni la revisione del curriculum gratis e riservata.
oppure trascina qui un file PDF, DOC, DOCX, ODT o PAGES di non oltre 5 MB.