Job Description About PSC Biotech Who are we?
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 candidate will provide documentation (creating, formatting, tracking of SOPs, Work Instructions etc in the Electronic Document Management Systems) support to the Vaccines IPT team and the role will be reporting to the Vaccines IPT Associate Director.
Requirements Responsibilities: Creating, editing, and formatting of SOPs, Work Instructions, and other documents on the EDMS (Veeva Vault) from material supplied by the Vaccine IPT SMEs.
Liaison with key stakeholders e.g., Quality, Change Control, SMEs etc.
to ensure compliance, correctness, content, and delivery.
Lead the tracking and maintaining of the project document delivery schedules for the team (using Excel).
Engage with Change Control and the wider project team to ensure documents are prepared and updated in time for different stages of C&Q execution and production.
Provides to the site knowledge and experience in Quality Documentation Systems.
Responsible for use of the Site Documentation System including Issuance, reconciliation, storage, archiving and retrieval of cGMP documentation to support the manufacture & testing of our products.
Responsible for maintaining the Site Master file for current effective cGMP documents on site Uses knowledge to improve Quality Documentation Systems, solve problems, provide continuous improvement, and execute tasks.
Provides compliance contribution to project teams and leads small projects.
Makes decisions within guidelines and policies which impact own priorities and allocation of time to meet deadlines.
Part-take in cross-functional problem-solving teams for troubleshooting and investigations within Vaccines IPT Ensure compliance with site EHS policy, cGMP and other business regulations and support Technical IPT input to risk assessments, audits, regulatory inspections, and incident investigations.
Ensure the highest Quality, Compliance and Safety standards by participating and complying with our Manufacturing Division Quality Management System (QMS) requirements, including ownership, as relevant.
Skills Required: In order to excel in this role, you will need to have: 1-5 years' experience as a documentation specialist or equivalent in a pharmaceutical or a highly regulated environment.
Experience in maintaining and updating excel schedules and trackers for small projects.
Advanced PC skills such as Excel, Word, PowerPoint.
Stakeholder management of multi decision makers, colleagues, peers, and cross functional teams.
Knowledge and experience of GMP and GDP in a pharmaceutical environment.
Desirable: Demonstrated knowledge in more than one pharmaceutical and/or chemical manufacturing operation (e.g., Manufacturing, Quality, Engineering, Tech Services etc).
Desirable: Qualification in a biological science subject.
Desirable: Evidence of Continuous Personal Development.
#LI-DM2 Requirements 1-5 years' experience as a documentation specialist or equivalent in a pharmaceutical or a highly regulated environment.
Experience in maintaining and updating excel schedules and trackers for small projects.
Advanced PC skills such as Excel, Word, PowerPoint.