Total 5 it specialist job vacancies in carmona

Duties & Responsibilities:

• Collaborate with cross-functional teams, including R&D, marketing, and production, to develop new food products and improve existing ones.
• Conduct market research to identify trends, consumer preferences, and competitor activities to inform product development strategies.
• Assist in the formulation and testing of new recipes, ensuring products meet quality standards and customer expectations.
• Ensure that all products adhere to safety standards, quality specifications, and regulatory requirements.
• Conduct regular audits of the production process and work closely with the quality assurance team to identify and resolve any issues.
• Monitor product consistency and work on troubleshooting any deviations in quality or process.
• Provide technical support and product training to customers, distributors, and sales teams to ensure a clear understanding of product features and benefits.
• Address customer inquiries and complaints regarding product performance, quality, or usage, and work towards satisfactory resolutions.
• Develop and deliver product presentations, demonstrations, and training sessions to both internal teams and external clients.
• Analyze sales data, customer feedback, and market trends to identify opportunities for product improvement or new product development.
• Prepare detailed reports on product performance, including sales figures, customer satisfaction, and areas for improvement.
• Support the sales team with data-driven insights to enhance product positioning and market penetration.
• Stay informed about new ingredients, technologies, and manufacturing processes that could enhance product quality or reduce costs.
• Provide technical input on packaging, labeling, and product specifications to ensure they meet both company standards and customer expectations.

Job Scope:

1. Maintain site-wide compliance by ensuring all activities and documentation are current, effective and in-use.

2. Ensure all Internal and External Audit including Third Party Audit Preparations are complete.

3. Assist in supplier accreditation/qualification and ensure compliance to required

documentation

4. Support in ensuring management of all Quality Management System-related

documents.

Duties & Responsibilities:

1.) Responsible in monitoring and maintaining completeness of documentation in all GMP processes in the company.

2.) Ensures all documentation for supplier accreditation/qualification are complete and current in compliance to regulations and customer requirements.

3.) Ensure annual training requirement for the company is complied with.

4.) Support safekeeping of all documents registered under Document Control Center.

5.) Facilitate Internal Quality Audit Team and its functional activities

6.) Facilitate all external audits (Regulatory and Certifying bodies, Clients/Customers)

6.) Support in executing continuous improvement actions and projects

7.) Ensure compliance to cGMP/GDP, FDA, Halal, FSSC, customer and other regulatory and statutory requirements.

8.) Provide assistance in deviation investigation, robust CAPA identification and implementation.

1.) Registered Pharmacist for all licenses, certificates, and permits of Blaine Group of Companies.

2.) Copes with a 5-day regulatory closing and schedule deadline

3.) Reconcile records of regulatory and inter-company regulatory necessities;

4.) Verify, check, and maintain validities of LTOs, CPRs, CPNs, Permits of the ff

Regulatory Agencies:

- Food and Drug Administration

- Bureau of Animal Industry

- Philippine Drug Enforcement Agency

- Philippine National Police

- Fertilizer and Pesticide Agency (2022 onwards)

5.) Creates and submits monthly, semi-annual, and annual reports to the above-

mentioned Regulatory Agencies

6.) Check and sign dossiers for submission to Regulatory Agencies,

7.) Validate completeness of requirements as mandated by Regulatory Agency for

compliance,

8.) Checks completeness of requirements as mandated by Regulatory Agency for

compliance;

9.) Represents the Company on all Regulatory Bodies for accreditations and

compliances,

10.) Responds to customers' external regulatory issues.

11.) Check records of management and archiving of documents for regulatory

compliances.

12.) Recommends regulatory management measures,

13.) Creates, amends, and maintains Product Labels both for internal and external use

14.) Check records of management and archiving of documents for regulatory

Compliance

15.) Recommends regulatory management measures,

Position Summary:

The R&D Specialist supports and gives assistance to the R&D Team and collaborate with her/his co-worker on all products developed and formulated products, performance of daily R&D activities, maintains and monitor all documents related to the R&D processes.                                                             

Job Scope:

1. Assists in the research and development of new products and protocols
2. Material Qualification and Accreditation
3. Product Costing
4. Perform SAP (Systems Application Product) transactions as required to support SBUs directly linked to R&D processes
5. Consolidation and safe-keeping of researches and related studies
6. Re-formulation of products and redirection of manufacturing processes as needed
7. Generation/ Preservation and Revision (if needed) of Master Production Documents
8. Trouble Shooting of problems regarding materials, processes, products and other related activities

Duties & Responsibilities:

In-charge of the manufacturing process trouble-shooting activities such as but not limited to:

1. Re-processing with advance under-studies product formula and recommends        pertinent percentage inclusion level to the original formulation for commercial process manufacturing
2. Ensures that the following parameters are satisfied within the covered monitoring:
   1. Chemical analysis recovery is within the specified requirement
   2. Physical and testing conformity
   3. Commercial batching conform the re-processing guide;
   4. Stability, if necessary
   5. Compilation of test result/s and monitoring intact
3. Perform the SAP (Systems Application Product) transactions required for raw material reservation/requisition for developmental products and trial batches
4. Conducts study, review and pre-qualification of alternative source/s of applicable raw material substitution to existing component in the product formulation/s as a resolution to the identified trouble-shooting made and recommends accordingly
5. Performs research activities, the collation and orderly safe-keeping of the researched data information, hand-outs, or related dossiers that supports the commercial trouble-shooting or the recommended product enhancement or fortification of the existing product formula
6. Conducts supporting trial testing parallel to the commercially-identified trouble to rule out root-cause and recommends appropriate corrective actions/ Support on answering and investigation on product complaint
7. Prepares Master Production Documentation of all Re-processing formulation and the applicable registration to the Document Control Center (DCC)
8. Conducts pilot scale and production scale batch trials and technology transfer for new products developed
9. Plays vital role for the developmental project’s first three (3) commercial process validation protocol run and the applicable documentation and change control
10. Responsible for preparing the documents required by Regulatory for Product Registration
11. SOP Creation and Revision if needed
12. Collation and Preparation of Product Quality Review
13. Responsible for the updating of file record of the Master Batch Production Record (MBPR) and assures the complete attachment of the relevant supporting documents of the product dossier per envelope
14. Responsible for the requisition of the office and laboratory supplies pertinent to the department’s activities
15. In-charge of the Monthly Developmental Progress Reporting and the need to call for any related coordination meeting with the manufacturing related departments
16. Ensures safe-keeping and the corresponding inventory management of glass wares and RPDD Laboratory Equipment plus its preventive maintenance and calibration requirements
17. Authorized signatory for the following documents in the absence of the RDD Manager such as: Product Label, Costing Approval, MBPR/MPDR or its BPR/PDR approval, and any Raw/Packaging Material’s accreditation
18. Represents the Department for scheduled and unscheduled meetings and other technical presentation/ trainings or suppliers’ product presentation in the absence of R&D Manager

Position Summary:

Responsible for the conduct of audit of different units, for processing payment authorization requests, for ensuring the accuracy of sales commission pay-outs, for performing the surprised cash count of petty cash fund, for monitoring the status of cash advances and prompt deposit of post dated checks collected from customers

Job Scope:

1. Conducts period audit
2. Processes payment request
3. Validates and checks sales commission pay-outs
4. Performs surprised cash and merchandise inventory count
5. Monitors status of cash advances and prompt deposit of customers’ PDCs
6. Prepares required monthly reports
7. Performs other tasks that may be assigned from time to time.

Duties & Responsibilities:

1. Conducts periodic audit of different units of the company, and prepares a report on its result
2. Ensures that all payment authorization request are valid, fully supported and properly approved before processing
3. Validates and reviews accuracy of sales commission pay-outs
4. Performs periodic surprised cash count of petty cash funds
5. Monitors status of employees cash advances and reports long outstanding unliquidated cash advances
6. Ensures that all customers’ post dated checks collected are promptly deposited to appropriate company’s account/s, and prepares a report on the status of aforesaid PDCs
7. Files and safekeeps transaction documents