Quality Assurance Expert

Fidia Pharma; Abano Terme; On-site; EUR 30,000 - 35,000; Full time

Benefits offered by this job

Collective bonus

Company welfare

Access to training and coaching programs

Pension fund with company integration

Health fund

Staff discounts

Job summary

A pharmaceutical company in Abano Terme is seeking a Quality Assurance Expert on a temporary contract. The role involves managing validations, participating in audits, and supporting Regulatory Affairs. Candidates should have a relevant degree and excellent English skills. A competitive salary of €30,000–€35,000 is offered along with bonuses and training opportunities. Join a dynamic team dedicated to quality in the pharmaceutical sector.

Qualifications

• Previous experience in quality assurance in pharmaceutical, cosmetics or food sectors is a plus.

Responsibilities

• Manage the validation of Gamma Ray sterilization cycles.
• Manage the packaging validation and transport validation.
• Issue the PQR of medicinal products at defined frequencies.
• Participate in audits and inspections from customers and authorities.
• Support Regulatory Affairs and manage packaging validation studies.
• Issue and review quality documents (SOP, IO, etc.).
• Manage complaints from the market.

Skills

Problem solving

Negotiation skills

Excellent English (B2)

Good knowledge of Office Suite

Education

Degree in materials science or related fields

Job description

Join to apply for the Quality Assurance Expert role at Fidia Pharma

Founded in 1946, Fidia is an Italian multinational pharmaceutical company, with R&D, manufacturing, marketing and sales capabilities, and an extensive product portfolio, mainly based on Hyaluronic Acid, in strategic therapeutic areas such as Joint care, Eye care, Skin care, Specialty care, Health&Wellness care. Headquartered in Abano Terme (PD), Fidia extends its global reach through local partners and distributors in 120+ countries worldwide, as well as with wholly owned subsidiaries.

With the aim of strengthening the Quality Department, we are recruiting a

Quality Assurance Expert (temporary contract)

You’ll work with the team to produce documentation related to validation and quality risk management.

Main responsibilities:

• Manage the validation of Gamma Ray sterilization cycles.
• Manage the packaging validation and the transport validation.
• Issue the PQR of the medicinal products at the defined frequencies.
• Participate in audits and inspections received from customers and authorities and perform internal audit and audit to the suppliers.
• Support the Regulatory Affairs department and manage packaging validation studies.
• Issue and review the quality documents (SOP, IO, etc.).
• Manage the complaints from the market.

Requirements:

• Degree in materials science, materials engineering, chemistry, industrial chemistry, biology, biotechnology, pharmaceutical chemistry and technology, pharmacy or other scientific degrees.
• Previous experience of quality assurance in the pharmaceutical, cosmetics or food sectors is considered a plus.
• Excellent knowledge of English (level B2).
• Good knowledge of the Office Suite.
• Problem solving and negotiation skills, as well as ability to learn.

Our offer:

• Temporary maternity-replacement contract.
• “C” or “D” grading of Chemical Pharmaceutical National Collective Agreement, will be determined based on the candidate’s profile characteristics.
• Salary between € 30.000 and € 35.000.
• Collective Bonus and company Welfare.

In Fidia you will have unlimited access to training and coaching programs aligned with market best practices and opportunities for professional development through participation in internal job posting processes, pension fund with company integration and health fund, merit review and referral programs, company canteen, staff discounts and access to the flu vaccination campaign.

Fidia Farmaceutici promotes parity and inclusion in all its actions.

All people from the status of candidate to that of employee and throughout the duration of their employment relationship are entitled to the same opportunities and protections regardless of gender identity, sexual orientation, ethnicity, migration background, religion, nationality, age. All company procedures are therefore drafted in compliance with the principles expressed in the previous point; any divergences should be promptly brought to the attention of the People & Culture Department.

Seniority level

• Entry level

Employment type

• Full-time

Job function

• Quality Assurance

Industries

• Pharmaceutical Manufacturing

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