Regulatory Affairs Associate

3 weeks ago

Cavite City, Philippines Buscojobs Full time

Regulatory Affairs Associate jobs in Cavite

Legal Assistant

Posted today

Job Description

Work Setup: In-office | Molino, Bacoor, Cavite

About Us: Nexventra Corporation is a Philippine-based start-up business process outsourcing (BPO) company. We work closely with our sister company, Nexventra LLC in the U.S., to support law firms by building reliable and skilled remote teams. As a growing company, we value people who are eager to learn, adaptable, and committed to doing meaningful work in a supportive environment.

Position Overview: We are looking for a Legal Assistant to join our team. This is an entry-level position, and no prior experience is required. Fresh graduates are welcome to apply. If you're detail-oriented, intelligent, and a fast learner with good computer skills, this could be the start of your career in the legal support field.

Key Responsibilities:

  • Assist with preparing, formatting, and proofreading legal documents and correspondence.
  • Manage case files, digital records, and deadlines with accuracy.
  • Support attorneys and staff with administrative tasks such as scheduling and data entry.
  • Communicate with professionalism and attention to detail.
  • Learn and apply procedures to ensure smooth workflow.

Qualifications:

  • Fresh graduates and applicants with no experience are encouraged to apply.
  • Strong attention to detail and accuracy.
  • Fast learner who can work with minimal supervision.
  • Proficient in Microsoft Word and comfortable using Adobe tools.
  • Strong grammar, spelling, and proofreading skills.
  • Fluent in spoken and written English.
  • Problem-solving skills and willingness to learn new tasks quickly.

What We Offer:

  • Paid training provided
  • 13th month pay
  • Paid overtime
  • Performance bonus
  • SSS, Pag-IBIG, and PhilHealth contributions
  • Supportive and growth-oriented work environment
Regulatory Affairs Officer

Posted today

Job Description

About the role

Reporting to the Head of Regulatory Affairs, this full-time Regulatory Affairs Officer position at Square Pharmaceutical, Inc. is a crucial role within the company's Science & Technology team. Based in Carmona Cavite, this role will be responsible for ensuring Square Pharmaceutical's products meet all relevant regulatory requirements and guidelines.

What you'll be doing

  • Prepare and submit regulatory applications and documentation to governing bodies such as the FDA and EMA
  • Monitor changes in regulations and guidelines, and advise the business on the impact and required actions
  • Collaborate with cross-functional teams to ensure regulatory compliance throughout the product lifecycle
  • Lead regulatory inspections and audits, and manage any resulting corrective actions
  • Build and maintain strong relationships with key regulatory authorities
  • Contribute to the development and implementation of the company's regulatory strategy

What we're looking for

  • In-depth knowledge of global regulatory requirements and guidelines for pharmaceutical products
  • Excellent written and verbal communication skills, with the ability to translate complex regulatory information
  • Strong project management and problem-solving skills, with the ability to work independently
  • Graduate of BS Pharmacy (licensed or not welcome to apply)

What we offer

  • Dynamic, collaborative work environment with supportive colleagues

About us

Square Pharmaceutical, Inc. is a pharmaceutical company dedicated to developing and manufacturing high-quality medications. With a strong focus on innovation and quality, we are committed to advancing the standards of healthcare through our diverse portfolio of products and solutions.

If this role sounds like the perfect next step in your career, we encourage you to apply now.

Regulatory Affairs Staff / CEZ, Rosario, Cavite

Posted today

Job Description

• Bachelor’s Degree in Pharmacy
• Licensed Pharmacist (with or without work experience).
• Regulatory Knowledge: Understanding of ISO standards (ISO 13485) and FDA regulations (preferred for applicants with prior RA experience).
• Documentation and Compliance: Strong skills in technical writing and document management.
• Data Analysis and Reporting: Proficiency in Microsoft Excel, including advanced functions.
• Risk Management: Familiarity with risk assessment methodologies (e.g., FMEA), particularly for applicants with RA experience.
• QMS Knowledge: Experience with Quality Management Systems (preferred).
• CAPA/NCR Handling: Ability to manage Corrective and Preventive Actions (CAPA) and Non-Conformance Reports (NCR), especially for applicants with RA experience.

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