Our Careers

JOB OPENINGS

Come and join our journey towards excellence.

Scope (project based):

● Gap Analysis of current systems in place vs ISO requirements

● Develop and execute Implementation Plan for ISO 9001 Certification as Lead Project Manager

● Assist Management to ensure and prepare organizational readiness (also for associates); may include coaching of quality management processes, workshops and laying the foundation for a continuous KAIZEN process model

● Responsible for delivery of project milestones, budget,KPI setting and certification



Qualifications:

● Proven and successful track record of ISO 9001 implementations

● Industrial Engineering Graduate Degree; master of engineering is an advantage

● Six sigma green belt or blackbelt degree preferable

● Skilled in diagram software such as Microsoft visio, draw etc

● Proficient in applying FMEA and SWOT/SMART Analysis models

● Understanding of every Clause and Sub-Clause of ISO 9001:2015



Terms:

● Term based Service Contract

● Service fees and conditions are subject to mutual agreement

Please apply with a detailed CV detailing your personal details (Picture,DOB,Residence etc), career record with particular attention to executed ISO 9001 projects and achievements and degrees of education.

Roles and Responsibilities:

● Planning concepts by studying relevant information and materials

● Illustrating concepts by designing examples of art arrangements, size, type size and style and submitting them for approval

● Preparing finished art by operating necessary equipment and software

● Coordinating with outside agencies, art services, web designer, marketing, printers, and colleagues as necessary

● Contributing to team efforts by accomplishing tasks as needed

● Communicating about layout and design

● Prioritize and manage multiple projects within design specifications

● Able to execute brand packaging designs for pharmaceutical products

● Create social media content cards, information cards, and other marketing materials

● Creating a wide range of graphics and layouts for product illustrations company

● Reviewing final layouts and suggesting improvements when necessary



Qualifications:

● Bachelor’s degree in Graphic Design or related field

● Experience as graphic artist or in related field

● Demonstrable graphic design skills with a strong portfolio

● Proficiency with required desktop publishing tools, Photoshop, Sketch, and other graphic design software

● A strong eye for visual composition

● Effective time management skills and the ability to meet deadlines

● Understanding of marketing, production, corporate identity, product packaging, advertisements and multimedia design

● Experience with computer-aided design

● Excellent IT skills, especially with design and photo-editing software

The Regulatory Affairs Associate is responsible in the proper documentation of all necessary permits, intellectual property rights certificate and assist the Head of Regulatory Affairs in the development of new and existing products. This is a desk-based role, involving the close study of scientific and legal documents.

Roles and Responsibilities:

• Assistance to the RA Department, as needed

• Assist on product label review

• Assist on product registration upload in FDA portal

• Administrative responsibilities, product filing in server, scanning of documents, filing of hard copies

• Assist in the management of regulatory tools and database

• Support the product registration process in coordination with the Head of Regulatory Affairs

• Monitors Certifications, Licenses and other Documents validity

• Maintain internal regulatory systems, database & processes, relating to regulatory & ‎quality

• Liaise with stakeholders to any regulatory concerns applicable to the projects.

• Timely reporting to various stakeholders on the status of ongoing projects

• Assisting in internal audits and quality documentation

• Ensure accuracy and currency of records and regulatory information held in databases

• Performs other job-related duties and responsibilities as determined by immediate head and/or performs job related task that may arise as needed by the company

Qualifications:

• Must be a Licensed Pharmacist

• With at least 1 year of experience in Regulatory Affairs

• Knowledgeable in FDA application and compliance processing

• Experience in handling Food Products and Medical Devices is an advantage

• Familiar with ACTD, AVG and FDA regulations

• Knowledgeable in GMP and audit

• Ability to work independently but knows how to collaborate with the team

• With strong follow up, organization and prioritization skills

• Good verbal and written communication skills

• Has an effective analytical and critical thinking skills

• Must be flexible and able to perform multi-tasking

• Can start asap

• Willing to work on-site in Parañaque

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