Scientist (Supply Analytics)

About PSC Biotech Ltd

Who we are?

PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.

Take your Career to a new Level

PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry.We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting.

Employee Value Proposition

Employees are the heartbeat of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client s expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met.

Overview:

The successful candidate will report into Supply Analytical Sciences (SAS) Manager to execute analytical testing support to aid closure of investigations for sites in Europe. This role is the ideal opportunity for an Analytical Scientist with a strong technical background, strong problem-solving skill set and knowledge of cGMP to develop their career.

Responsibilities

• Execution of Analytical testing to support release of drug substance and drug product
  
• Execution of testing to support closure of investigations relating to extraneous matter investigations
  
• Author analytical procedures and technical reports.
  
• Complete Quality Risk Assessments.
  
• Execute analytical testing to support problem solving.
  
• Provide technical input during inspections and audits.
  
• Technical trouble shooting skills to perform analytical investigations and aid development of corrective / preventative actions
  

Requirements

Required Skills: Have a working knowledge of:

• Completion of laboratory work using a variety of analytical techniques (eg optical and scanning electron microscopy, FTIR spectroscopic methods, liquid chromatography, gas chromatography) to support drug substance and drug product release and aid investigations.
  
• Understanding of GMP testing and laboratory investigation requirements
  
• Data integrity and recent Pharmaceutical industry trends.
  
• Ability to execute laboratory testing to meet agreed deadlines and work with customers in sites in Europe and colleagues in US laboratories
  

Demonstrate strong verbal and written communication skills and ability to work in a team environment.

Demonstrate strong interpersonal skills flexibility and sensitivity in working with different cultures.

Self motivated to take ownership and accountability of issues and drive them to completion.

Ability to speak up and raise issues and help to drive to resolution.

Ability to quickly adapt to changes and develop appropriate plans for managing risks.

Qualifications

Required: MSc. degree in Analytical Science or BSc. Degree in science with Minimum 2 years Analytical Science experience.

Preferred: Experience in pharmaceutical Quality Control analytical laboratory.