RMA Consultants
2 months ago
Drug Substance SME (Contract- Pharmaceutical)
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Company information
- Company
- RMA Consultants
- Location
- Singapore Singapore
- Posted
- 2 months ago
Job description
Our Client is a multinational Pharma and Biotech leader constructing a billion dollar ADC manufacturing facility in Singapore.
SCOPE OF WORK
- Engineering design support for mAbs Process which may include
- Process equipment incl SU Bioreactors, chromatography and TFF skids
- Buffer and Media Prep systems incl. filling stations, vessels and transfer lines
- CIP skids and distribution.
- Central Dispensing and Logistics for DS activities
- Support / coordination for DS Process utilities
- Work closely with the Designers ( Exyte & Pharmadule Morimatsu ) to develop the design, translating AZ technical requirements into the agreed engineering deliverables.
- Work closely with the site operations team and global support such as GTO (as necessary) to have an aligned AZ position on critical technical areas and communicate with Exyte design team in a single unified manner
- Attend all necessary design discussions and provide technical direction to AZ requirements and drive a risk based ’design to cost’ ethos into the design decision making process for your areas of responsibility
- Coach and support Exyte design team to develop User Requirement Specifications (URSs) that are technically complete (eg. CTQs, GMP, GEP and SHE requirements), technically correct and appropriate for C&Q execution
- Review and approve all URSs within technical area as Engineering SME Approver (engineering requirements)
- Review and comment on assigned engineering deliverables produced by Exyte & equipment suppliers.
- Attend supplier visits for critical equipment packages (on as required basis)
- Carry out periodic Design Assurance reviews and reporting (30,60,90%), to ensure ongoing technical alignment and identification of value engineering opportunities.
- Provide technical support to SHE risk assessments (HAZOPs, SWIFT, LOPA studies etc.) and ensure key risks are identified and appropriate mitigations are included in the design.
- Work collaboratively with assigned Work Package Owners to ensure the technically compliant delivery of equipment packages Attend supplier visits for critical/ancillary equipment packages (depending on geography and carbon budget considerations)
- Participate in and make recommendations for the procurement strategy for technical work packages including pre-qualification/contractor selection and technical content/scope of contracts.
- Review and comment of BD Design Deliverables within required review periods ( with support as required from GTO SME)
- Review and approve DQ protocols for critical equipment packages as they become available
- Ensuring SHE considerations, sustainability targets, relevant SME engagement and AZ standards are incorporated into proposed solutions
- Work collaboratively with assigned Work Package owners and C&Q partners to ensure the technically compliant delivery of equipment packages.
- In addition to SME duties, start to pick up the responsibilities as mAbs SME for the project as GTO support is curtailed in June down to an ad-hoc level from Q3 onwards
If you are keen to know more about this role, please email Mary at [email protected] and send your resume in MS Word format. Note that only shortlisted candidates will be contacted.
Required skills
- logistics
- bioreactors
- swift
- pharmaceutical
- contract
- chromatography
- engineering design
- technical areas
- singapore
- value engineering
- technical requirements
- risk mitigation
- biotech
- media preparation
- dispensing
- site operations
- procurement strategy
- design to cost
- technical direction
- pre-qualification
- engineering deliverables
- equipment suppliers
- design discussions
- hazops
- technical content
- buffer preparation
- equipment packages
- process utilities
- design deliverables
- contractor selection
- sustainability targets
- adc manufacturing
- mabs
- tff skids
- cip skids
- drug substance (ds)
- global technical operations (gto)
- user requirement specifications (urss)
- critical to quality (ctqs)
- good manufacturing practice (gmp)
- good engineering practice (gep)
- safety, health, and environment (she) requirements
- commissioning & qualification (c&q)
- engineering sme approver
- design assurance reviews
- she risk assessments
- lopa studies
- work package owners
- scope of contracts
- design qualification (dq) protocols
- az standards
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