Key factors at a glance
- Seniority
- Mid
- Experience
- 2+ years
- Work mode
- On-site
- Salary
- Not stated
- Required working language
- English
Must-haves
- University degree in relevant scientific discipline
- 1-3 years of experience in pharmaceutical or biopharmaceutical sector
- Excellent written and verbal communication skills
- Proficient in Microsoft Word, Excel, and PowerPoint
- Ability to work in accordance with GMP practices
- Experience in providing technical support
Nice-to-haves
- Independent in assignments
- Experience leading projects or supervising teams
- Knowledge of EHS policies
- Experience in laboratory documentation review
- Ability to adjust procedures and processes
Company hiring signal
See whether Alvotech is scaling up or slowing down, from its posting history.
Original posting
EnglishQA Specialist - Product Testing Review We are seeking a QA Specialist to join our QA Product Testing Review team. In this role, the candidate will independently review and approve laboratory documentation supporting product release, in-process, and stability testing in accordance with GDP requirements in a GMP-regulated pharmaceutical or biopharmaceutical environment. Scope and Responsibilities: • Review and complete laboratory documentation (support stability, product in-process and release testing) . • Inform about review issues. • Provide technical support where required. • Being able to work in accordance with GMP practices, conducting all activities in a compliant manner. • Provide expertise in selected analytical techniques and thorough understanding and overview of all analytical methods applied for product testing and stability testing. • Being aware of and comply with Alvotech’s current EHS policies. • Support deviations and investigations as required. • Provide support during inspections as required. • Being independent in assignments. Routinely lead projects and/or supervise small or medium teams of technicians or admin. • Perform both routine tasks within procedures and processes and non-routine tasks. Take part in large projects. • Challenges and decisions are discussed, made and solved in cooperation with supervisor/other employees. • Can make adjustments/changes to procedures, processes and projects. • Can have financial impact through decision making. • Demonstrate expert knowledge within field of expertise such as methods, techniques and equipment as well as relevant procedural/process knowledge. • Being often an advisory to other less experienced employees. • Apply good documentation practices when completing records. Minimum education and experience requirements: • Education and experience: University degree in a relevant scientific discipline and minimum 1-3 years of relevant experience in pharmaceutical or biopharmaceutical sector. • Communication skills: Excellent written and verbal communication skills, coordination abilities and good team skills. • Computer literacy: Proficient in use of a PC and common Microsoft packages such as Word, Excel and PowerPoint. What we offer: • An inspiring challenge to work with great co-workers on ambitious projects that change people's lives. • The chance to be a part of a global and fast-growing company. • An international work culture that encourages diversity, collaboration and inclusion. • Positive, flexible, and innovative work environment. • Support for personal growth and internal career development. • Company social events and milestone celebrations. • Excellent in-house canteen and coffee house. • Exercise and wellbeing support for full-time employees. • On-site shower facility. • Transportation grant towards eco-friendly modes of travel for full-time employees. • Internet at home for full-time employees.
Shown in its original English. To apply, continue to the company's own page.