At Singa, the entrepreneurial atmosphere allows everyone to actively innovate and work hard to take the initiative and achieve outstanding results.We recognize that talent is our most important asset and we offer the training, education and growth opportunities to take your career to the next level. 

Here, you will meet people who are better than yourself, and move from good to great together.

OPEN POSITIONS

Sales Manager

Job Description

To develop business in South East Asia region

To maintain key account by providing customized solution to the customer, improve the quality and service continuously.

To guide and lead a sales team in the region.

Tender/bidding preparation.

 

Operation Manager

Job Description

Requirement

More than 5 Years working experience in pharmaceutical supply chain management, or logistics packaging material management.

Strong communication and negotiation skill.

Bachelor Degree and above.

To manage the production in Singapore as well as the regional warehouse management.

Product quality improvement continuously and maintain safety inventory level.

To find opportunity to lower operation cost.

Daily production and warehouse operation.

Requirement

Leadership, at least 5 years people management experience in logistics/production sites.

Strong team spirit, good communication skill

Bachelor Degree and above.

Senior Validation Engineer

Job Description

The Senior Validation Engineer is responsible creating and executing computer system and cold chain validation and regulated cold chain operating  SOP and documentation to assure compliance across the technical portfolio of Singa and thus ensure conformance to cGxPs, guidance documents, and applicable industry accepted standards.

1.Provide interpretation, guidance, and training regarding qualification and validation requirements in a  GxP environment, including 21CFR11, Predicate Rules and General Principles of Software Validation (such as GAMP 5 Compliance).

2.Participate in software platform project teams and author, review and approve

computer and cold chain validation related documentation including but not limited to: risk assessments, validation plan, user requirements, specifications, UAT, traceability matrix, testing (IQ/OQ/PQ), data migration, qualification/validation protocols and validation summery reports.

3.Participate/lead in the review of current and future SDLC/CSV policies and procedures.

4.Support initiatives related to audit readiness, management of internal/external audits as well as regulatory inspections, and responding to findings in areas of responsibility.

5.Demonstrate strong proficiency in applying established tools and methods (for example, Six Sigma, Lean) to identify and realize new product or process introductions, as well as process and business improvements.

6.Implement, and/or maintain process software quality control plans that are in accordance with product or process risk level, and ensures those plans are consistently followed.

7.Actively coach talent across the tech organization on quality principles.

8.Partner with business SMEs and training to prepare user documentation and training materials.

Requirement

1.5+ years IT software testing and validation experience of increasing project size and complexity.     

2.Strongly preferred experience within the pharmaceutical logistics and cold chain industry.

3.Bachelor's degree, specialization in IT or Management Information Systems (MIS) preferred.

4.Strong knowledge of FDA regulations and experience in implementing 21 CFR Part 11 and regulated Software Development Life Cycles.

5.nowledge of CSV requirements (IQ/OQ/PQ).

6.Strong analytical skills ,ability and desire to work in a fast pace, dynamic environment.

7.Strong Time Management, Organization and Execution Skills,strong written, verbal and presentation communication skills.

8.Strong collaboration skills required to effectively work across a diverse group including executives, managers and Subject Matter Experts (SME).Effective interpersonal and conflict resolution skills.