QC Specialist-Biopharma

FRS Recruitment; Limerick; On-site; EUR 55,000 - 70,000; Full time

Benefits offered by this job

Yearly bonuses

Pension

Enhanced annual leave days

Medical health care cover

Dental cover

Life Insurance

Share Option Scheme

Flexible work pattern

Job summary

FRS Recruitment is partnering with a biologics company in the Mid-West region to appoint a QC Specialist. The role involves supporting equipment qualification, method transfer and routine in-process and release testing within the QC labs on a range of projects focused on manufacturing biological products for early-phase clinical trials.

Ideal candidates will have a Biochemistry/Biological Sciences/Chemistry degree and 5–6 years’ GMP biologics QC experience, with hands-on expertise in HPLC,

Qualifications

• Relevant degree in Biochemistry, Biological Sciences, Chemistry.
• 5–6 years min industry experience in GMP biologics QC.
• Knowledge and practical experience with analytical assays such as HPLC, Capillary Electrophoresis and PCR.

Responsibilities

• Participate in method validation and/ or technical transfer execution.
• Serve as a technical expert to develop, qualify, validate and troubleshoot HPLC, Capillary Electrophoresis, PCR and Cell culture assays.
• Ensure all aspects of QC work comply to GMP standards.
• Create and approve SOPs, report forms and specifications.

Skills

HPLC

Capillary Electrophoresis

PCR

Cell culture

GMP

SOP development

Education

Biochemistry / Biological Sciences / Chemistry degree

Job description

QC Specialist FRS Recruitment are delighted to be partnering with a biologics company in the Mid -West Region to recruit for a QC Specialist. As the QC Specialist you will be participating in and providing subject matter expertise in equipment qualification, method transfer and routine in-process and release testing within the QC labs, in addition to other QC-supporting is a great opportunity for an experienced Analytical QC professional that is keen to take a step into a unique role where they will work on a range of projects focused on manufacturing of biological products at early phase clinical trials.

KEY DUTIES AND RESPONSIBILITIES

Your duties as the QC Specialist will be varied however the key duties and responsibilities are as follows:

• Participate in method validation and/ or technical transfer execution as needed.
• Serve as a technical expert to develop, qualify, validate and troubleshoot HPLC, Capillary Electrophoresis, PCR and Cell culture assays.
• You will ensure all aspects of QC work comply to GMP standards.
• You will create and approve SOPs, report forms and specifications.

ROLE REQUIREMENTS

To be successful in your application to this exciting opportunity as the QC Specialist we are looking to identify the following on your profile and work history:

• Relevant degree in Biochemistry, Biological Sciences, Chemistry.
• 5-6 years min industry experience working in a GMP biologics facility, specifically in a QC department.
• Knowledge and practical experience with analytical assays such as HPLC, Capillary Electrophoresis and PCR.

Hours of work : Days only : 8.30am to 4.30pm Mon -Fri

WHAT'S ON OFFER

• Flexible work pattern
• Yearly Bonuses
• Share Option Scheme
• Pension
• Enhanced annual leave days
• Medical Health care cover
• Dental cover
• Life Insurance

Key words:

Scientist, Bioassay Scientist, Bioassay Analyst Biopharma Scientist, Biopharmaceutical analyst, Biochemist, Biochemistry, Chemist, analytical Chemist, Stability analyst, Biochemist, Biochemistry, Chemist, analytical Chemist, Stability analyst, Biochemist, Biochemistry, Chemist, analytical Chemist, Stability analyst, Biochemist, Biochemistry, Chemist, analytical Chemist.

The company are not in a position to support sponsorship for this role.

Skills: GMP HPLC PCR Audit Benefits: Benefits TPBN1_IJ